Keratoconus
Corneal Topography
Keratoplasty, Penetrating
Cornea
Corneal Stroma
Aberrometry
Corneal Transplantation
Astigmatism
Fuchs' Endothelial Dystrophy
Epikeratophakia
Visual Acuity
Riboflavin
Eye Proteins
Zernike representation of corneal topography height data after nonmechanical penetrating keratoplasty. (1/337)
PURPOSE: To demonstrate a mathematical method for decomposition of discrete corneal topography height data into a set of Zernike polynomials and to demonstrate the clinical applicability of these computations in the postkeratoplasty cornea. METHODS: Fifty consecutive patients with either Fuchs' dystrophy (n = 20) or keratoconus (n = 30) were seen at 3 months, 6 months, and 1 year (before suture removal) and again after suture removal following nonmechanical trephination with the excimer laser. Patients were assessed using regular keratometry, corneal topography (TMS-1, simulated keratometry [SimK]), subjective refraction, and best-corrected visual acuity (VA) at each interval. A set of Zernike coefficients with radial degree 8 was calculated to fit two model surfaces: a complete representation (TOTAL) and a representation with parabolic terms only to define an approximate spherocylindrical surface (PARABOLIC). The root mean square error (RMS) was calculated comparing the corneal raw height data with TOTAL (TOTALRMS) and PARABOLIC (PARABOLICRMS). The cylinder of subjective refraction was correlated with the keratometric readings, the SimK, and the respective Zernike parameter. Visual acuity was correlated with the tilt components of the Zernike expansion. RESULTS: The measured corneal surface could be approximated by the composed surface 1 with TOTALRMS < or = 1.93 microm and by surface 2 with PARABOLICRMS < or = 3.66 microm. Mean keratometric reading after suture removal was 2.8+/-0.6 D. At all follow-up examinations, the SimK yielded higher values, whereas the keratometric reading and the refractive cylinder yielded lower values than the respective Zernike parameter. The correlation of the Zernike representation and the refractive cylinder (P = 0.02 at 3 months, P = 0.05 at 6 months and at 1 year, and P = 0.01 after suture removal) was much better than the correlation of the SimK and refractive cylinder (P = 0.3 at 3 months, P = 0.4 at 6 months, P = 0.2 at 1 year, and P = 0.1 after suture removal). Visual acuity increased from 0.23+/-0.10 at the 3-month evaluation to 0.54+/-0.19 after suture removal. After suture removal, there was a statistically significant inverse correlation between VA and tilt (P = 0.02 in patients with keratoconus and P = 0.05 in those with Fuchs' dystrophy). CONCLUSIONS: Zernike representation of corneal topography height data renders a reconstruction of clinically relevant corneal topography parameters with a marked reduction of redundance and a small error. Correlation of amount/axis of refractive cylinder with respective Zernike parameters is more accurate than with keratometry or respective SimK values of corneal topography analysis. (+info)Visual function after penetrating keratoplasty for keratoconus: a prospective longitudinal evaluation. (2/337)
AIMS: To evaluate visual function and vision specific health status in patients undergoing penetrating keratoplasty for keratoconus. METHODS: A prospective longitudinal study measuring logMAR visual acuity, contrast sensitivity, disability glare, binocular visual field, stereoacuity, and subjective visual function (VF-14) was conducted on 18 patients with keratoconus undergoing penetrating keratoplasty (PK), including six patients who had already had PK in the fellow eye. Data were collected preoperatively and at 3, 9, and 18 months after surgery. RESULTS: Within 3 months of surgery there was significant improvement in aided visual acuity, contrast sensitivity, and stereoacuity (p<0.05); disability glare (p<0.05) no longer had a significant detrimental effect on these variables. VF-14 score improved significantly throughout the postoperative period (p<0.05). There was significant correlation of the VF-14 score with aided visual acuity, binocular visual field, and stereoacuity. Postoperative astigmatism (<4D v >4D) did not affect the VF-14 score significantly. CONCLUSIONS: There is substantial and rapid improvement in visual function and vision specific health status in keratoconic patients as a result of uncomplicated penetrating keratoplasty. (+info)Acute hydrops in the corneal ectasias: associated factors and outcomes. (3/337)
PURPOSE: To identify factors associated with the development of hydrops and affecting its clinical outcome. METHODS: Chart review of all patients with acute hydrops seen by a referral cornea service during a 2.5-year period between June 1996 and December 1998. RESULTS: Twenty-one patients (22 eyes) with acute hydrops were seen. Nineteen patients had keratoconus, 2 had pellucid marginal degeneration, and 1 had keratoglobus. Twenty-one of 22 (95%) eyes had seasonal allergies and 20 of 22 (91%) eyes had allergy-associated eye-rubbing behavior. Six of 22 (27%) had a diagnosis of Down's syndrome. Six patients were able to identify a traumatic inciting event: vigorous eye rubbing in 4 and traumatic contact lens insertion in 2. The affected area ranged from 7% to 100% of the corneal surface area and was related to disease duration and final visual acuity. Proximity of the area of edema to the corneal limbus ranged from 0 to 2.3 mm and was also related to prognosis. Three serious complications were observed: a leak, an infectious keratitis, and an infectious keratitis and coincidental neovascular glaucoma. Various medical therapies did not differ significantly in their effect on outcome, and ultimately 4 (18%) of 22 patients underwent penetrating keratoplasty. Best-corrected visual acuity was equal to or better than prehydrops visual acuity in 5 of the 6 patients in whom prehydrops visual acuity was known, without corneal transplantation. CONCLUSIONS: Allergy and eye-rubbing appear to be important risk factors in the development of hydrops. Visual results are acceptable in some patients without surgery. Close observation allows for the early detection and treatment of complications such as perforation and infection. (+info)A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13. (4/337)
PURPOSE: A two-generation consanguineous Pakistani family with autosomal recessive Leber congenital amaurosis (LCA, MIM 204,000) and keratoconus was identified. All affected individuals have bilateral keratoconus and congenital pigmentary retinopathy. The goal of this study was to link the disease phenotype in this family. METHODS: Genomic DNA was amplified across the polymorphic microsatellite poly-CA regions identified by markers. Polymerase chain reaction (PCR) products were separated by nondenaturing polyacrylamide gel electrophoresis. Alleles were assigned to individuals, which allowed calculation of LOD scores using the Cyrillic and MLINK software program. The retinal guanylate cyclase (RETGC-1, GDB symbol GUC2D) and pigment epithelium-derived factor (PEDF) genes were analyzed by heteroduplex analysis and direct sequencing for mutations in diseased individuals. RESULTS: Based on a whole genome linkage analysis the first locus for this combined phenotype has been mapped to chromosome 17p13. Linkage analysis gave a two point LOD score of 3.21 for marker D17S829. Surrounding this marker is a region of homozygosity of 15.77 cM, between the markers D17S1866 and D17S960; however, the crossover for the marker D17S1529 refines the region to 10.77 cM within which the disease gene is predicted to lie. Mutation screening of the nearby RETGC-1 gene, which has been shown to be associated with LCA1, revealed no mutations in the affected individuals of this family. Similarly, another prime candidate in the region PEDF was also screened for mutations. The factor has been shown to be involved in the photoreceptor differentiation and neuronal survival. No mutations were found in this gene either. Furthermore, RETGC-1 was physically excluded from the critical disease region based on the existing physical map. CONCLUSIONS: It is therefore suggested that this combined phenotype maps to a new locus and is due to an as yet uncharacterized gene within the 17p13 chromosomal region. (+info)Graft failure in human donor corneas due to transmission of herpes simplex virus. (5/337)
AIM: To report the clinical consequences of contamination of human donor corneas by herpes simplex virus (HSV) in organ culture. METHODS: Two patients without previous history of ocular HSV infection underwent penetrating keratoplasty (PK), one for keratoconus and the other for Fuchs' endothelial dystrophy. One patient suffered primary graft failure while the other developed a persistent epithelial defect, ultimately resulting in graft failure. Viral culture of swabs taken from both corneas during the early postoperative period was undertaken. The failed donor corneas were examined histopathologically by immunohistochemistry (IHC) for HSV-1 antigens, transmission electron microscopy (TEM), and by polymerase chain reaction (PCR) for HSV DNA. Both failed corneas were replaced within 6 weeks of the initial surgery. The records of the fellow donor corneas were also examined for evidence of infection. RESULTS: HSV was cultured from both corneas during the early postoperative period. Histology of both donor corneas demonstrated a thickened corneal stroma with widespread necrosis of keratocytes and loss of endothelial cells. IHC showed keratocytes positive with antibodies to HSV-1 antigens. TEM demonstrated HSV-like viral particles within degenerating keratocytes. PCR performed on the failed corneal grafts was positive for HSV-1 DNA, whereas PCR performed on the excised host corneal buttons was negative in both patients. Records of the fellow donor corneas showed that one cornea was successfully transplanted into another recipient after 18 days in organ culture, whilst the other was discarded because of extensive endothelial cell necrosis noted after 15 days in organ culture. CONCLUSION: HSV within a donor cornea may cause endothelial destruction in organ culture and both primary graft failure and ulcerative keratitis after transplantation. Endothelial necrosis of a donor cornea in culture also raises the possibility of HSV infection within the fellow cornea. (+info)Atopy and keratoconus: a multivariate analysis. (6/337)
BACKGROUND/AIMS: The primary goal of this study was to determine if atopy is a risk factor for keratoconus. Other potential risk factors were also studied and included age, sex, race, eye rubbing, mitral valve prolapse, handedness, collagen vascular disease, ocular trauma, pigmentary retinopathy, Marfan's syndrome, Down's syndrome, and a history of contact lens wear. METHODS: A case-control study was designed (n=120) with incident cases assembled from the years 1985-99. Controls were chosen from the same person-time experience as cases and were picked from a source population with multiple outcomes ensuring that none was knowingly related to any of the potential exposures being studied. Atopy was defined based on the UK working group 1994 definition (at least 4/6 criteria = complete, 3/6 criteria = incomplete, and at least 1/6 criteria = partial). Keratoconus was defined based on clinical criteria and previously published I-S values. Multiple logistic regression was used in the analysis to obtain the odds ratios as the measure of association. RESULTS: In the univariate associations, there was an association between keratoconus and atopy as well as eye rubbing and family history of keratoconus. However, in the multivariate analysis, only eye rubbing was still a significant predictor of keratoconus (odds ratio = 6.31 p = 0.001). CONCLUSIONS: This study supports the hypothesis that the most significant cause of keratoconus is eye rubbing. Atopy may contribute to keratoconus but most probably via eye rubbing associated with the itch of atopy. No other variable measured was significantly associated with the aetiology of keratoconus. (+info)Corneal endothelial cell apoptosis in patients with Fuchs' dystrophy. (7/337)
PURPOSE: To investigate whether apoptosis plays a notable role in degeneration of corneal endothelial cells in patients with Fuchs' dystrophy. METHODS: Forty-seven corneal buttons from 41 patients with Fuchs' dystrophy were studied. Nucleus labeling, transmission electron microscopy (TEM), and TdT-dUTP terminal nick-end labeling (TUNEL) were used to detect apoptosis. TEM and TUNEL were performed on sections of all 47 corneal buttons, and nucleus labeling was performed on the last 10 corneas. Seven human donor corneas, two corneal buttons from two patients with keratoconus, and one corneal button from a patient with interstitial keratitis were used as negative controls for detection of apoptotic endothelial cells. Negative controls were studied by means of nucleus labeling, TUNEL, and TEM. RESULTS: In the nucleus labeling assay, the average percentage of apoptotic endothelial cells was 2.65% in the Fuchs' dystrophy group (n = 10) and 0.23% in the control group (n = 10; P = 0.0003). In the TUNEL assay, labeling of some endothelial cells was observed on 42 of 47 corneas in the Fuchs' dystrophy group, whereas it was absent on most specimens of the control group. In TEM, most endothelial cell nuclei had a normal appearance, and apoptotic endothelial cells featuring condensed nucleus and decreased cell size could be observed exceptionally. Some apoptotic cells were found in the basal epithelial cell layer by means of nucleus labeling, TUNEL, and TEM in the Fuchs' dystrophy group but not in the control group. CONCLUSIONS: This study suggests that apoptosis plays an important role in endothelial cell degeneration in Fuchs' dystrophy. Because of a lack of conclusive evidence of increased endothelial apoptosis by TEM, further studies are needed to ascertain this finding. (+info)The paretic pupil: its incidence and aetiology after keratoplasty for keratoconus. (8/337)
The present study reveals that pupillary abnormalities are common after keratoplasty for keratoconus and that, in addition to the fixed dilated pupils which we have found in 7.8 per cent. of eyes, varying degrees of partially dilated pupil frequently occur after operation. In our experience, glaucoma is not a sequel to the simple paretic pupil, a finding which confirms the results of the smaller series of Alberth and Schnitzler (1971); glaucoma thus seems to be no more a special complication of keratoplasty for keratoconus than it is of keratoplasty for any other corneal pathology. The paretic pupils can be explained on the basis of ischaemic atrophy of the sphincter pupillae muscle secondary to an iris strangulation phenomenon occurring during surgery in the manner we have discussed. The relative frequency of a dilated pupil, together with the common finding of focal iris atrophy after minimal surgical trauma to the iris in cases of keratoconus, forces one to conclude that the pathology in this condition is not confined to the cornea but probably extends to the iris and possibly to the scleral envelope as well. (+info)Keratoconus is a degenerative non-inflammatory disorder of the eye, primarily affecting the cornea. It is characterized by a progressive thinning and steepening of the central or paracentral cornea, causing it to assume a conical shape. This results in irregular astigmatism, myopia, and scattering of light leading to blurred vision, visual distortions, and sensitivity to glare. The exact cause of keratoconus is unknown, but it may be associated with genetics, eye rubbing, and certain medical conditions. It typically starts in the teenage years and progresses into the third or fourth decade of life. Treatment options include glasses, contact lenses, cross-linking, and corneal transplantation in advanced cases.
Corneal topography is a non-invasive medical imaging technique used to create a detailed map of the surface curvature of the cornea, which is the clear, dome-shaped surface at the front of the eye. This procedure provides valuable information about the shape and condition of the cornea, helping eye care professionals assess various eye conditions such as astigmatism, keratoconus, and other corneal abnormalities. It can also be used in contact lens fitting, refractive surgery planning, and post-surgical evaluation.
Penetrating keratoplasty (PK) is a type of corneal transplant surgery where the entire thickness of the host's damaged or diseased cornea is removed and replaced with a similar full-thickness portion of a healthy donor's cornea. The procedure aims to restore visual function, alleviate pain, and improve the structural integrity of the eye. It is typically performed for conditions such as severe keratoconus, corneal scarring, or corneal ulcers that cannot be treated with other, less invasive methods. Following the surgery, patients may require extended recovery time and rigorous postoperative care to minimize the risk of complications and ensure optimal visual outcomes.
The cornea is the clear, dome-shaped surface at the front of the eye. It plays a crucial role in focusing vision. The cornea protects the eye from harmful particles and microorganisms, and it also serves as a barrier against UV light. Its transparency allows light to pass through and get focused onto the retina. The cornea does not contain blood vessels, so it relies on tears and the fluid inside the eye (aqueous humor) for nutrition and oxygen. Any damage or disease that affects its clarity and shape can significantly impact vision and potentially lead to blindness if left untreated.
The corneal stroma, also known as the substantia propria, is the thickest layer of the cornea, which is the clear, dome-shaped surface at the front of the eye. The cornea plays a crucial role in focusing vision.
The corneal stroma makes up about 90% of the cornea's thickness and is composed of parallel bundles of collagen fibers that are arranged in regular, repeating patterns. These fibers give the cornea its strength and transparency. The corneal stroma also contains a small number of cells called keratocytes, which produce and maintain the collagen fibers.
Disorders that affect the corneal stroma can cause vision loss or other eye problems. For example, conditions such as keratoconus, in which the cornea becomes thin and bulges outward, can distort vision and make it difficult to see clearly. Other conditions, such as corneal scarring or infection, can also affect the corneal stroma and lead to vision loss or other eye problems.
Corneal pachymetry is a medical measurement of the thickness of the cornea, which is the clear, dome-shaped surface at the front of the eye. This measurement is typically taken using a specialized instrument called a pachymeter. The procedure is quick, painless, and non-invasive.
Corneal pachymetry is an essential test in optometry and ophthalmology for various reasons. For instance, it helps assess the overall health of the cornea, identify potential abnormalities or diseases, and determine the correct intraocular lens power during cataract surgery. Additionally, corneal thickness is a crucial factor in determining a person's risk for developing glaucoma and monitoring the progression of the disease.
In some cases, such as with contact lens fitting, corneal pachymetry can help ensure proper fit and minimize potential complications. Overall, corneal pachymetry is an essential diagnostic tool in eye care that provides valuable information for maintaining eye health and ensuring appropriate treatment.
Contact lenses are thin, curved plastic or silicone hydrogel devices that are placed on the eye to correct vision, replace a missing or damaged cornea, or for cosmetic purposes. They rest on the surface of the eye, called the cornea, and conform to its shape. Contact lenses are designed to float on a thin layer of tears and move with each blink.
There are two main types of contact lenses: soft and rigid gas permeable (RGP). Soft contact lenses are made of flexible hydrophilic (water-absorbing) materials that allow oxygen to pass through the lens to the cornea. RGP lenses are made of harder, more oxygen-permeable materials.
Contact lenses can be used to correct various vision problems, including nearsightedness, farsightedness, astigmatism, and presbyopia. They come in different shapes, sizes, and powers to suit individual needs and preferences. Proper care, handling, and regular check-ups with an eye care professional are essential for maintaining good eye health and preventing complications associated with contact lens wear.
Aberrometry is a medical diagnostic technique used to measure the amount and type of aberration or distortion in the optical system of the eye. It is often used to evaluate the quality of vision, particularly in cases where traditional methods of measuring visual acuity are not sufficient.
During an aberrometry test, the patient looks into a specialized instrument called a wavefront sensor while a series of light patterns are projected onto the retina. The sensor then measures how the light is distorted as it passes through the eye's optical system, including the cornea and lens. This information is used to create a detailed map of the eye's aberrations, which can help doctors identify any irregularities that may be contributing to visual symptoms such as blurred vision, glare, or halos around lights.
Aberrometry is often used in conjunction with other diagnostic tests to evaluate patients who are considering refractive surgery, such as LASIK or PRK. By identifying any abnormalities in the eye's optical system, doctors can determine whether a patient is a good candidate for surgery and make more informed decisions about how to proceed with treatment.
Corneal transplantation, also known as keratoplasty, is a surgical procedure in which all or part of a damaged or diseased cornea is replaced with healthy corneal tissue from a deceased donor. The cornea is the clear, dome-shaped surface at the front of the eye that plays an important role in focusing vision. When it becomes cloudy or misshapen due to injury, infection, or inherited conditions, vision can become significantly impaired.
During the procedure, the surgeon carefully removes a circular section of the damaged cornea and replaces it with a similarly sized piece of donor tissue. The new cornea is then stitched into place using very fine sutures that are typically removed several months after surgery.
Corneal transplantation has a high success rate, with more than 90% of procedures resulting in improved vision. However, as with any surgical procedure, there are risks involved, including infection, rejection of the donor tissue, and bleeding. Regular follow-up care is essential to monitor for any signs of complications and ensure proper healing.
Corneal diseases are a group of disorders that affect the cornea, which is the clear, dome-shaped surface at the front of the eye. The cornea plays an important role in focusing vision, and any damage or disease can cause significant visual impairment or loss. Some common types of corneal diseases include:
1. Keratoconus: A progressive disorder in which the cornea thins and bulges outward into a cone shape, causing distorted vision.
2. Fuchs' dystrophy: A genetic disorder that affects the inner layer of the cornea called the endothelium, leading to swelling, cloudiness, and decreased vision.
3. Dry eye syndrome: A condition in which the eyes do not produce enough tears or the tears evaporate too quickly, causing discomfort, redness, and blurred vision.
4. Corneal ulcers: Open sores on the cornea that can be caused by infection, trauma, or other factors.
5. Herpes simplex keratitis: A viral infection of the cornea that can cause recurrent episodes of inflammation, scarring, and vision loss.
6. Corneal dystrophies: Inherited disorders that affect the structure and clarity of the cornea, leading to visual impairment or blindness.
7. Bullous keratopathy: A condition in which the endothelium fails to pump fluid out of the cornea, causing it to swell and form blisters.
8. Corneal trauma: Injury to the cornea caused by foreign objects, chemicals, or other factors that can lead to scarring, infection, and vision loss.
Treatment for corneal diseases varies depending on the specific condition and severity of the disease. Options may include eyedrops, medications, laser surgery, corneal transplantation, or other treatments.
Astigmatism is a common eye condition that occurs when the cornea or lens has an irregular shape, causing blurred or distorted vision. The cornea and lens are typically smooth and curved uniformly in all directions, allowing light to focus clearly on the retina. However, if the cornea or lens is not smoothly curved and has a steeper curve in one direction than the other, it causes light to focus unevenly on the retina, leading to astigmatism.
Astigmatism can cause blurred vision at all distances, as well as eye strain, headaches, and fatigue. It is often present from birth and can be hereditary, but it can also develop later in life due to eye injuries or surgery. Astigmatism can be corrected with glasses, contact lenses, or refractive surgery such as LASIK.
Fuchs' Endothelial Dystrophy is a medical condition that affects the eye's cornea. It is a slowly progressing disorder that causes the endothelium, a thin layer of cells lining the inner surface of the cornea, to deteriorate and eventually fail to function properly. This results in swelling of the cornea, leading to cloudy vision, distorted vision, and sensitivity to light.
The condition is typically inherited and tends to affect both eyes. It is more common in women than in men and usually becomes apparent after the age of 50. There is no cure for Fuchs' Endothelial Dystrophy, but treatments such as corneal transplantation can help improve vision and alleviate symptoms.
Epikeratophakia is a surgical procedure used in ophthalmology to correct vision problems, particularly astigmatism. It involves grafting a thin layer of donor corneal tissue, called a lenticule, onto the surface of the recipient's cornea using a special adhesive. The donor tissue is usually shaped to correct the specific irregularities in the recipient's cornea that are causing the vision problem.
The procedure is typically performed as an outpatient procedure and takes about 30 minutes to complete. After the surgery, patients may experience some discomfort, light sensitivity, and blurred vision for a few days, but these symptoms usually resolve within a week or two.
Epikeratophakia has been largely replaced by newer procedures such as LASIK and PRK, which offer similar results with fewer risks and faster recovery times. However, it may still be used in certain cases where other procedures are not suitable, such as in patients with thin corneas or severe dry eye.
Visual acuity is a measure of the sharpness or clarity of vision. It is usually tested by reading an eye chart from a specific distance, such as 20 feet (6 meters). The standard eye chart used for this purpose is called the Snellen chart, which contains rows of letters that decrease in size as you read down the chart.
Visual acuity is typically expressed as a fraction, with the numerator representing the testing distance and the denominator indicating the smallest line of type that can be read clearly. For example, if a person can read the line on the eye chart that corresponds to a visual acuity of 20/20, it means they have normal vision at 20 feet. If their visual acuity is 20/40, it means they must be as close as 20 feet to see what someone with normal vision can see at 40 feet.
It's important to note that visual acuity is just one aspect of overall vision and does not necessarily reflect other important factors such as peripheral vision, depth perception, color vision, or contrast sensitivity.
An Eye Bank is an organization that collects, stores, and distributes donated human eyes for corneal transplantation and other ocular medical research purposes. The eye bank's primary function is to ensure the quality of the donated tissue and make it available for those in need of sight-restoring procedures.
The cornea, the clear front part of the eye, can be surgically transplanted from a deceased donor to a recipient with corneal damage or disease, thereby improving or restoring their vision. The eye bank's role includes obtaining consent for donation, retrieving the eyes from the donor, evaluating the tissue for suitability, preserving it properly, and then allocating it to surgeons for transplantation.
Eye banks follow strict medical guidelines and adhere to ethical standards to ensure the safety and quality of the donated tissues. The process involves screening potential donors for infectious diseases and other conditions that may affect the quality or safety of the cornea. Once deemed suitable, the corneas are carefully removed, preserved in specific solutions, and stored until they are needed for transplantation.
In addition to corneal transplants, eye banks also support research and education in ophthalmology by providing human eye tissues for various studies aimed at advancing our understanding of eye diseases and developing new treatments.
Riboflavin, also known as vitamin B2, is a water-soluble vitamin that plays a crucial role in energy production and cellular function, growth, and development. It is essential for the metabolism of carbohydrates, fats, and proteins, and it helps to maintain healthy skin, hair, and nails. Riboflavin is involved in the production of energy by acting as a coenzyme in various redox reactions. It also contributes to the maintenance of the mucous membranes of the digestive tract and promotes iron absorption.
Riboflavin can be found in a variety of foods, including milk, cheese, leafy green vegetables, liver, kidneys, legumes, yeast, mushrooms, and almonds. It is sensitive to light and heat, so exposure to these elements can lead to its degradation and loss of vitamin activity.
Deficiency in riboflavin is rare but can occur in individuals with poor dietary intake or malabsorption disorders. Symptoms of riboflavin deficiency include inflammation of the mouth and tongue, anemia, skin disorders, and neurological symptoms such as confusion and mood changes. Riboflavin supplements are available for those who have difficulty meeting their daily requirements through diet alone.
Ocular refraction is a medical term that refers to the bending of light as it passes through the optical media of the eye, including the cornea and lens. This process allows the eye to focus light onto the retina, creating a clear image. The refractive power of the eye is determined by the curvature and transparency of these structures.
In a normal eye, light rays are bent or refracted in such a way that they converge at a single point on the retina, producing a sharp and focused image. However, if the curvature of the cornea or lens is too steep or too flat, the light rays may not converge properly, resulting in a refractive error such as myopia (nearsightedness), hyperopia (farsightedness), or astigmatism.
Ocular refraction can be measured using a variety of techniques, including retinoscopy, automated refraction, and subjective refraction. These measurements are used to determine the appropriate prescription for corrective lenses such as eyeglasses or contact lenses. In some cases, ocular refractive errors may be corrected surgically through procedures such as LASIK or PRK.
Prosthesis implantation is a surgical procedure where an artificial device or component, known as a prosthesis, is placed inside the body to replace a missing or damaged body part. The prosthesis can be made from various materials such as metal, plastic, or ceramic and is designed to perform the same function as the original body part.
The implantation procedure involves making an incision in the skin to create a pocket where the prosthesis will be placed. The prosthesis is then carefully positioned and secured in place using screws, cement, or other fixation methods. In some cases, tissue from the patient's own body may be used to help anchor the prosthesis.
Once the prosthesis is in place, the incision is closed with sutures or staples, and the area is bandaged. The patient will typically need to undergo rehabilitation and physical therapy to learn how to use the new prosthesis and regain mobility and strength.
Prosthesis implantation is commonly performed for a variety of reasons, including joint replacement due to arthritis or injury, dental implants to replace missing teeth, and breast reconstruction after mastectomy. The specific procedure and recovery time will depend on the type and location of the prosthesis being implanted.
Eye proteins, also known as ocular proteins, are specific proteins that are found within the eye and play crucial roles in maintaining proper eye function and health. These proteins can be found in various parts of the eye, including the cornea, iris, lens, retina, and other structures. They perform a wide range of functions, such as:
1. Structural support: Proteins like collagen and elastin provide strength and flexibility to the eye's tissues, enabling them to maintain their shape and withstand mechanical stress.
2. Light absorption and transmission: Proteins like opsins and crystallins are involved in capturing and transmitting light signals within the eye, which is essential for vision.
3. Protection against damage: Some eye proteins, such as antioxidant enzymes and heat shock proteins, help protect the eye from oxidative stress, UV radiation, and other environmental factors that can cause damage.
4. Regulation of eye growth and development: Various growth factors and signaling molecules, which are protein-based, contribute to the proper growth, differentiation, and maintenance of eye tissues during embryonic development and throughout adulthood.
5. Immune defense: Proteins involved in the immune response, such as complement components and immunoglobulins, help protect the eye from infection and inflammation.
6. Maintenance of transparency: Crystallin proteins in the lens maintain its transparency, allowing light to pass through unobstructed for clear vision.
7. Neuroprotection: Certain eye proteins, like brain-derived neurotrophic factor (BDNF), support the survival and function of neurons within the retina, helping to preserve vision.
Dysfunction or damage to these eye proteins can contribute to various eye disorders and diseases, such as cataracts, age-related macular degeneration, glaucoma, diabetic retinopathy, and others.
The Descemet membrane is the thin, transparent basement membrane that is produced by the corneal endothelial cells. It is located between the corneal stroma and the corneal endothelium, which is the innermost layer of the cornea. The Descemet membrane provides structural support for the corneal endothelium and helps to maintain the proper hydration and clarity of the cornea. It is named after the French physician Jean Descemet, who first described it in 1752.