Fraser Syndrome
Syndactyly
Frasier Syndrome
Abnormalities, Multiple
Extracellular Matrix Proteins
Salmon
British Columbia
Expression of Fraser syndrome genes in normal and polycystic murine kidneys. (1/4)
(+info)Basement membrane assembly of the integrin alpha8beta1 ligand nephronectin requires Fraser syndrome-associated proteins. (2/4)
(+info)fras1 shapes endodermal pouch 1 and stabilizes zebrafish pharyngeal skeletal development. (3/4)
(+info)Sprouty1 haploinsufficiency prevents renal agenesis in a model of Fraser syndrome. (4/4)
(+info)Fraser Syndrome is a rare genetic disorder characterized by a combination of congenital anomalies, including cryptophthalmos (abnormal development of the eyes leading to complete or partial covering by the skin), syndactyly (fusion of fingers and/or toes), urogenital abnormalities, and hearing loss. Other features may include laryngeal and tracheal abnormalities, nasolacrimal duct obstruction, and developmental delay. The syndrome is caused by mutations in the FRAS1 or FREM2 genes and is inherited in an autosomal recessive manner.
Syndactyly is a congenital condition where two or more digits (fingers or toes) are fused together. It can occur in either the hand or foot, and it can involve fingers or toes on both sides of the hand or foot. The fusion can be partial, where only the skin is connected, or complete, where the bones are also connected. Syndactyly is usually noticed at birth and can be associated with other genetic conditions or syndromes. Surgical intervention may be required to separate the digits and improve function and appearance.
Eyelids are the thin folds of skin that cover and protect the front surface (cornea) of the eye when closed. They are composed of several layers, including the skin, muscle, connective tissue, and a mucous membrane called the conjunctiva. The upper and lower eyelids meet at the outer corner of the eye (lateral canthus) and the inner corner of the eye (medial canthus).
The main function of the eyelids is to protect the eye from foreign particles, light, and trauma. They also help to distribute tears evenly over the surface of the eye through blinking, which helps to keep the eye moist and healthy. Additionally, the eyelids play a role in facial expressions and non-verbal communication.
A syndrome, in medical terms, is a set of symptoms that collectively indicate or characterize a disease, disorder, or underlying pathological process. It's essentially a collection of signs and/or symptoms that frequently occur together and can suggest a particular cause or condition, even though the exact physiological mechanisms might not be fully understood.
For example, Down syndrome is characterized by specific physical features, cognitive delays, and other developmental issues resulting from an extra copy of chromosome 21. Similarly, metabolic syndromes like diabetes mellitus type 2 involve a group of risk factors such as obesity, high blood pressure, high blood sugar, and abnormal cholesterol or triglyceride levels that collectively increase the risk of heart disease, stroke, and diabetes.
It's important to note that a syndrome is not a specific diagnosis; rather, it's a pattern of symptoms that can help guide further diagnostic evaluation and management.
I'm sorry for any confusion, but "Frasier Syndrome" is not a recognized medical condition or syndrome in the standard medical literature. It seems like it might be a term that is specific to a certain context or fictional work. In popular culture, "Frasier" is a television show about a character named Frasier Crane, and it's possible that "Frasier Syndrome" could refer to something within the realm of that fiction. However, without more specific information about where you encountered this term, I cannot provide an accurate definition.
'Abnormalities, Multiple' is a broad term that refers to the presence of two or more structural or functional anomalies in an individual. These abnormalities can be present at birth (congenital) or can develop later in life (acquired). They can affect various organs and systems of the body and can vary greatly in severity and impact on a person's health and well-being.
Multiple abnormalities can occur due to genetic factors, environmental influences, or a combination of both. Chromosomal abnormalities, gene mutations, exposure to teratogens (substances that cause birth defects), and maternal infections during pregnancy are some of the common causes of multiple congenital abnormalities.
Examples of multiple congenital abnormalities include Down syndrome, Turner syndrome, and VATER/VACTERL association. Acquired multiple abnormalities can result from conditions such as trauma, infection, degenerative diseases, or cancer.
The medical evaluation and management of individuals with multiple abnormalities depend on the specific abnormalities present and their impact on the individual's health and functioning. A multidisciplinary team of healthcare professionals is often involved in the care of these individuals to address their complex needs.
Eye abnormalities refer to any structural or functional anomalies that affect the eye or its surrounding tissues. These abnormalities can be present at birth (congenital) or acquired later in life due to various factors such as injury, disease, or aging. Some examples of eye abnormalities include:
1. Strabismus: Also known as crossed eyes, strabismus is a condition where the eyes are misaligned and point in different directions.
2. Nystagmus: This is an involuntary movement of the eyes that can be horizontal, vertical, or rotatory.
3. Cataracts: A cataract is a clouding of the lens inside the eye that can cause vision loss.
4. Glaucoma: This is a group of eye conditions that damage the optic nerve and can lead to vision loss.
5. Retinal disorders: These include conditions such as retinal detachment, macular degeneration, and diabetic retinopathy.
6. Corneal abnormalities: These include conditions such as keratoconus, corneal ulcers, and Fuchs' dystrophy.
7. Orbital abnormalities: These include conditions such as orbital tumors, thyroid eye disease, and Graves' ophthalmopathy.
8. Ptosis: This is a condition where the upper eyelid droops over the eye.
9. Color blindness: A condition where a person has difficulty distinguishing between certain colors.
10. Microphthalmia: A condition where one or both eyes are abnormally small.
These are just a few examples of eye abnormalities, and there are many others that can affect the eye and its functioning. If you suspect that you have an eye abnormality, it is important to consult with an ophthalmologist for proper diagnosis and treatment.
Extracellular matrix (ECM) proteins are a group of structural and functional molecules that provide support, organization, and regulation to the cells in tissues and organs. The ECM is composed of a complex network of proteins, glycoproteins, and carbohydrates that are secreted by the cells and deposited outside of them.
ECM proteins can be classified into several categories based on their structure and function, including:
1. Collagens: These are the most abundant ECM proteins and provide strength and stability to tissues. They form fibrils that can withstand high tensile forces.
2. Proteoglycans: These are complex molecules made up of a core protein and one or more glycosaminoglycan (GAG) chains. The GAG chains attract water, making proteoglycans important for maintaining tissue hydration and resilience.
3. Elastin: This is an elastic protein that allows tissues to stretch and recoil, such as in the lungs and blood vessels.
4. Fibronectins: These are large glycoproteins that bind to cells and ECM components, providing adhesion, migration, and signaling functions.
5. Laminins: These are large proteins found in basement membranes, which provide structural support for epithelial and endothelial cells.
6. Tenascins: These are large glycoproteins that modulate cell adhesion and migration, and regulate ECM assembly and remodeling.
Together, these ECM proteins create a microenvironment that influences cell behavior, differentiation, and function. Dysregulation of ECM proteins has been implicated in various diseases, including fibrosis, cancer, and degenerative disorders.
I'm sorry for any confusion, but "Salmon" is not a medical term. It is a common name for various species of fish that belong to the family Salmonidae and are known for their distinctive pink or red flesh. They are an important source of food and are popular in many cuisines around the world. If you have any questions about medical terminology, I'd be happy to help with those instead!
British Columbia is a province located on the west coast of Canada. It is not a medical term or concept. The province has a diverse geography, with mountains, forests, and coastal areas. Its largest city is Vancouver, and its capital is Victoria. The province is known for its natural beauty and outdoor recreational opportunities, as well as its vibrant cities and cultural attractions. It is home to a number of medical facilities and healthcare providers, and the provincial government plays a role in regulating and funding healthcare services within the province.
Fraser syndrome
Vaginal anomalies
FRAS1
Raymond Horton-Smith Prize
Glutamate receptor-interacting protein
PDZ domain
Branchio-oto-renal syndrome
Jim Swire
FREM2
George R. Fraser
Clitoromegaly
Vaginal atresia
Cryptophthalmos
Iain Macintyre
Jules François
Cervicocranial syndrome
1q21.1 deletion syndrome
Cortes Lacassie syndrome
Tethered spinal cord syndrome
Infertility in polycystic ovary syndrome
Failed back syndrome
List of diseases (M)
Frasier (disambiguation)
Ralf Adams
List of diseases (S)
Coffin-Lowry syndrome
White woman of Gippsland
Axenfeld-Rieger syndrome
Christophe Fraser
Primary ovarian insufficiency
Fraser syndrome - Wikipedia
Can you see with Fraser syndrome? - Curvesandchaos.com
Fraser Syndrome 3 | Hereditary Ocular Diseases
FVDSS4 · Fraser Valley Down Syndrome Society
Funding Available · Fraser Valley Down Syndrome Society
White-nose syndrome (Pseudogymnoascus destructans) | Fraser Valley Invasive Species Society
Share it: Characteristic dental pattern with hypodontia and short roots in Fraser syndrome
Motionographer® politics
Fras1 MGI Mouse Gene Detail - MGI:2385368 - Fraser extracellular matrix complex subunit 1
Branchiootorenal/branchiootic syndrome: MedlinePlus Genetics
Eyelid Coloboma: Practice Essentials, Background, Pathophysiology
MedlinePlus - Search Results for: Hypoplastic male external genitalia
Eyelid Coloboma Differential Diagnoses
urofacial syndrome - Ontology Browser - Rat Genome Database
Surveys and Measures | DPCPSI
Richard L. Huganir - Publications
Renal Agenesis/Hypoplasia | NCBDDD | CDC
Frasier Syndrome (definition)
Alzheimer Disease in Down Syndrome: Overview, Pathophysiology/Risk Factors, Epidemiology
Preauricular Sinuses Clinical Presentation: History, Physical Examination
Visual Snow Syndrome: Symptoms, Causes, and Treatment
Ccnb1ip1 Mouse Gene Details | cyclin B1 interacting protein 1 | International Mouse Phenotyping Consortium
Irritable Bowl Syndrome | Visual.ly
Tushar Desai's Profile | Stanford Profiles
Alumni Profile David Wotherspoon - Psychology - Simon Fraser University
Let's change how we look at Imposter Syndrome
Measles, Mumps, and Rubella -- Vaccine Use and Strategies for Elimination of Measles, Rubella, and Congenital Rubella Syndrome...
Serotonin Syndrome: Practice Essentials, Problem, Management
Unsere Publikationen & Bücher
Melnick-Fraser1
- Look for major anomalies and minor anomalies - renal agenesis is seen in hundreds of genetic conditions, including common trisomies, deletion 22q11, Melnick-Fraser syndrome, Fraser cryptophthalmos syndrome, and branchio-oto-renal syndrome. (cdc.gov)
Cryptophthalmos syndrome1
- 1986) also emphasized the occurrence of the cryptophthalmos syndrome without cryptophthalmos and proposed diagnostic criteria for Fraser syndrome. (wikipedia.org)
Mutations9
- Fraser syndrome is caused by mutations in three different genes : FRAS1, GRIP1, and FREM2 and is inherited in an autosomal recessive manner. (curvesandchaos.com)
- Fraser syndrome 1 ( 219000 ) results from homozygous mutations in the FRAS1 gene. (arizona.edu)
- Fraser syndrome 2 ( 617666 ) is caused by homozygous mutations in the FREM2 gene. (arizona.edu)
- Mutations in three genes, EYA1 , SIX1 , and SIX5 , have been reported in people with BOR/BO syndrome. (medlineplus.gov)
- SIX5 gene mutations have been found in a small number of people with BOR syndrome, although researchers question whether mutations in this gene cause the condition. (medlineplus.gov)
- Fraser Syndrome, characterized by mutations in the FRAS/FREM protein family, presents a variety of manifestations, ranging from epidermal blistering to renal disorders. (medscape.com)
- [ 3 ] Although mutations in FRAS1 or FREM2 genes appear in half of Fraser syndrome cases, the syndrome's expression can vary significantly among individuals. (medscape.com)
- Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1. (medscape.com)
- Mutations in this gene are associated with Fraser syndrome. (utsouthwestern.edu)
Abnormalities15
- Eye abnormalities typically lead to impairment or loss of vision in people with Fraser syndrome. (curvesandchaos.com)
- The prenatal ultrasound can reveal features like polyhydramnios or oligohydramnios, echogenic lungs, renal abnormalities or agenesis and cryptophthalmos that are pathognomonic of the Fraser Syndrome. (curvesandchaos.com)
- Kabuki syndrome is a rare genetic disorder with a range of characteristics, including intellectual disability, distinctive facial features and skeletal abnormalities. (curvesandchaos.com)
- Fraser syndrome is characterized by multiple physical abnormalities. (curvesandchaos.com)
- Branchiootic (BO) syndrome includes many of the same features as BOR syndrome, but affected individuals do not have kidney abnormalities. (medlineplus.gov)
- most people with BOR/BO syndrome have hearing loss and other ear abnormalities. (medlineplus.gov)
- BOR syndrome (but not BO syndrome) causes abnormalities of kidney structure and function. (medlineplus.gov)
- and a syndrome that includes preauricular sinuses, conductive deafness, commissural lip pits, and external ear abnormalities. (medscape.com)
- This results in abnormalities such as trisomies (Down, Edwards, and Patau syndrome) or abnormalities in the sex chromosomes (including Klinefelter, Turner, Jacobs, and Triple X syndrome). (nipt-geneplanet.com)
- Fraser syndrome is an autosomal recessive malformation disorder characterized by cryptophthalmos, syndactyly, and abnormalities of the respiratory and urogenital tract (summary by van Haelst et al. (beds.ac.uk)
- Because data on Brazilian women with polycystic ovary syndrome (PCOS) are still scarce, a nation-wide collaborative study was designed to determine the prevalence of metabolic and reproductive abnormalities and the presence of anxiety and depression in Brazilian women with PCOS. (bmj.com)
- Fetal Alcohol Syndrome (FAS) was first defined in 1973 as a condition characterized by pre- and postnatal growth deficiencies, facial abnormalities, and defects of the central nervous system . (asu.edu)
- Branchiootic syndrome is a rare, genetic multiple congenital anomalies syndrome characterized by second branchial arch anomalies (branchial cysts and fistulae), malformations of the outer, middle and inner ear associated with sensorineural, mixed or conductive hearing loss, and the absence of renal abnormalities. (mendelian.co)
- Eyes can be absent, deformed, or incompletely developed at birth, often in conjunction with other congenital abnormalities and syndromes. (msdmanuals.com)
- Coloboma of the iris raises the possibility of CHARGE association ( c oloboma, h eart defects, a tresia of the choanae, r etardation of mental and/or physical development, g enital hypoplasia, and e ar abnormalities), cat eye syndrome, Kabuki syndrome, or Aicardi syndrome. (msdmanuals.com)
Congenital7
- Fraser syndrome (also known as Meyer-Schwickerath's syndrome, Fraser-François syndrome, or Ullrich-Feichtiger syndrome) is an autosomal recessive congenital disorder, identified by several developmental anomalies. (wikipedia.org)
- Fraser syndrome (FS) is a rare autosomal recessive multiple congenital malformation syndrome characterized by cryptophthalmos, cutaneous syndactyly, renal agenesis, ambiguous genitalia, and laryngotracheal anomalies. (uni-halle.de)
- [ 4 ] Goldenhar syndrome, on the other hand, might manifest an eyelid coloboma and is linked with a myriad of other conditions like cleft lip, congenital heart defects, and scoliosis. (medscape.com)
- This statement summarizes the goals and current strategies for measles, rubella, and congenital rubella syndrome (CRS) elimination and for mumps reduction in the United States. (cdc.gov)
- U.S. Public Health Service year 2000 objectives include eliminating measles, rubella, and congenital rubella syndrome, and reducing mumps incidence to less than 500 reported cases per year. (cdc.gov)
- See Bowen syndrome (211200) for a comparable but probably distinct syndrome of multiple congenital malformations. (beds.ac.uk)
- Adetailedhistorywastakenand hadenlargedclitorisand1(7.1%)had cally.Althoughhormonal,genetic,mo- physicalexaminationandscreeningfor hypoplasticclitorisandvagina(Fraser lecularandradiographicinvestigations pituitaryhormones(thyroidstimulat- syndrome);6patientshadlabialfusion areneededtodeterminetheetiology, inghormone,adrenocorticotropichor- (42.9%)(Table1).Nogonadswere physicalexaminationremainsakeyfor mone(ACTH)andgonadotropins) palpableinanyofthem.Congenital diagnosis[ 2 ],particularlycarefulpalpa- were conducted. (who.int)
FRAS11
- In 2 families with Fraser syndrome unlinked to the FRAS1 gene, Jadeja et al. (wikipedia.org)
Anomalies4
- In about half of all cases of bilateral renal agenesis there are other structural anomalies (e.g. urogenital, cardiac, skeletal, central nervous system) or syndromes (chromosomal or genetic). (cdc.gov)
- New familial syndrome of unilateral upper eyelid coloboma, aberrant anterior hairline pattern, and anal anomalies in Manitoba Indians. (medscape.com)
- Branchiootorenal (BOR) syndrome is characterized by branchial arch anomalies (branchial clefts, fistulae, cysts), hearing impairment (malformations of the auricle with pre-auricular pits, conductive or sensorineural hearing impairment), and renal malformations (urinary tree malformation, renal hypoplasia or agenesis, renal dysplasia, renal cysts). (mendelian.co)
- and Aarskog syndrome (with limb and genital anomalies). (msdmanuals.com)
Upper eyelid coloboma3
- [ 10 ] Lastly, the Manitoba Oculotrichoanal (MOTA) syndrome is distinguished by features such as unilateral upper eyelid coloboma and a bifid nose. (medscape.com)
- Yeung A, Amor D, Savarirayan R. Familial upper eyelid coloboma with ipsilateral anterior hairline abnormality: two new reports of MOTA syndrome. (medscape.com)
- Of the 19 cases of upper eyelid coloboma, 5 occurred in isolation, 11 were associated with facial deformities, and 3 were part of a first arch syndrome (according to the Mustarde classification). (medscape.com)
Diagnosis7
- An earlier pregnancy had resulted in the intrauterine death at 30 weeks of gestation of a male fetus with a normal karyotype in whom the diagnosis of Fraser syndrome was suggested by the presence of cryptophthalmos, syndactyly, ambiguous genitalia, imperforate anus, bilateral renal agenesis, pulmonary hypoplasia, and hydrocephalus. (wikipedia.org)
- citation needed] The diagnosis of this syndrome can be made on clinical examination and perinatal autopsy. (wikipedia.org)
- The diagnosis of Fraser syndrome should be entertained in patients with a combination of acrofacial and urogenital malformations with or without cryptophthalmos. (wikipedia.org)
- The prenatal diagnosis of Fraser Syndrome is frequently possible. (curvesandchaos.com)
- The utility of these criteria notwithstanding, diagnosis of serotonin syndrome can be challenging, particularly in the perioperative setting. (medscape.com)
- NMS is the condition most commonly cited in the differential diagnosis when serotonin syndrome is a concern. (medscape.com)
- Who have identified diagnosis such as Cerebral Palsy, Down Syndrome, Autism. (fvcdc.org)
Families with Fraser syndrome3
- In 6 of 18 consanguineous families with Fraser syndrome, van Haelst et al. (wikipedia.org)
- citation needed] In 5 families with Fraser syndrome, McGregor et al. (wikipedia.org)
- citation needed] Among 18 consanguineous families with Fraser syndrome, van Haelst et al. (wikipedia.org)
Frontonasal dysplasia1
- Median cleft face syndrome or frontonasal dysplasia: a case report with associated kidney malformation. (medscape.com)
Malformation1
- Fraser syndrome and cryptophthalmos: review of the diagnostic criteria and evidence for phenotypic modules in complex malformation syndromes. (medscape.com)
Autosomal dominant3
- BOR/BO syndrome is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. (medlineplus.gov)
- A novel autosomal dominant syndrome consisting of hypertelorism, punctal pits, preauricular sinus, and deafness (HPPD) located on 14q31 has been noted. (medscape.com)
- An eyelid coloboma is an almost constant feature of Treacher Collins syndrome, which is autosomal dominant with variable penetrance and expressivity. (medscape.com)
Coloboma4
- [ 6 ] CHARGE syndrome presents a suite of symptoms including coloboma, heart defects, and growth retardation. (medscape.com)
- [ 9 ] Nasopalpebral Lipoma Coloboma syndrome brings with it peculiarities like an upper eyelid lipoma and underdeveloped maxilla. (medscape.com)
- Babu NS, Raviprakash D, Kumar R. Nasopalpebral lipoma coloboma syndrome. (medscape.com)
- Coloboma of the eyelid is frequently associated with epibulbar dermoid cysts and is common in Treacher Collins syndrome, Nager syndrome, and Goldenhar syndrome. (msdmanuals.com)
Frasier Syndrome2
- How common is Frasier Syndrome? (curvesandchaos.com)
- What is Frasier syndrome? (curvesandchaos.com)
Branchiootorenal2
- Branchiootorenal (BOR) syndrome is a condition that disrupts the development of tissues in the neck and causes malformations of the ears and kidneys. (medlineplus.gov)
- The two conditions are otherwise so similar that researchers often consider them together (BOR/BO syndrome or branchiootorenal spectrum disorders). (medlineplus.gov)
Characterized by cryptophthalmos1
- Fraser syndrome is a rare, autosomal recessive disorder characterized by cryptophthalmos, syndactyly, and renal agenesis or obstructive uropathy.100 The cryptophthalmos is present in 85% and is bilateral in 70% of these cases. (curvesandchaos.com)
Kabuki1
- What is Kabuki syndrome? (curvesandchaos.com)
Genetic4
- Fraser syndrome is an autosomal recessive genetic disorder. (curvesandchaos.com)
- The resulting genetic changes affect the development of organs and tissues before birth, which leads to the characteristic features of BOR/BO syndrome. (medlineplus.gov)
- Genetic or chromosomal testing if syndrome suspected. (cdc.gov)
- Bannayan-Riley-Ruvalcaba syndrome is a genetic condition characterised by a large head (macrocephaly), multiple noncancerous tumours and tumour-like growths called hamartomas, and dark freckles on the penis in males. (nipt-geneplanet.com)
Deletion1
- The NIFTY test technology, however, scans all chromosomes and can detect 60 deletion and duplication syndromes. (nipt-geneplanet.com)
Delleman-Oorthuys1
- [ 8 ] In contrast, Delleman-Oorthuys syndrome is known for cerebral and orbital cysts alongside facial or eye tags. (medscape.com)
Goldenhar Syndrome1
- Goldenhar Syndrome - ophthalmologist's perspective. (medscape.com)
Characteristic1
- What are the physical findings characteristic of Fraser syndrome? (curvesandchaos.com)
Genes1
- Some people with BOR/BO syndrome do not have an identified mutation in any of the genes listed above. (medlineplus.gov)
GONADAL DYSGENESIS1
- A syndrome characterized by CHRONIC KIDNEY FAILURE and GONADAL DYSGENESIS in phenotypic females with karyotype of 46,XY or female individual with a normal 46,XX karyotype. (reference.md)
Geneticist1
- Fraser syndrome is named for the geneticist George R. Fraser, who first described the syndrome in 1962. (wikipedia.org)
Chromosome1
- 2003) located the Fraser syndrome locus to chromosome 4q21. (wikipedia.org)
Findings2
- The authors noted that the findings in the sibs were consistent with classic Fraser syndrome. (wikipedia.org)
- Serotonin syndrome can manifest with findings that range from benign to fatal. (medscape.com)
Prevalence1
- What is the prevalence of Fraser syndrome? (curvesandchaos.com)
Defects1
- Hemifacial microsomia syndrome can include preauricular sinuses, facial nerve palsy, sensorineural hearing loss, microtia or anotia, cervical appendages containing cartilage, and other defects. (medscape.com)
Clinical6
- 2007) concluded that a phenotype resembling AMS is a rare clinical expression of Fraser syndrome, with no obvious genotype/phenotype correlation. (wikipedia.org)
- Phenotypic spectrum of CHARGE syndrome based on clinical characteristics. (medscape.com)
- Individuals with DS or trisomy 21 develop a clinical syndrome of dementia with clinical and neuropathologic characteristics almost identical to those of AD as described in individuals without DS. (medscape.com)
- Serotonin syndrome can have a variety of clinical presentations, but the majority of cases manifest within 24 hours of a change of dose or initiation of a drug. (medscape.com)
- Cat eye syndrome (CES) is a rare chromosomal disorder with a highly variable clinical presentation. (nipt-geneplanet.com)
- Severe acute respiratory syndrome in Singapore : clinical features of index patient and initial contacts. (cdc.gov)
Cleft2
- In people with BOR/BO syndrome, abnormal development of the second branchial arch can result in the formation of masses in the neck called branchial cleft cysts. (medlineplus.gov)
- They may involve only a single, specific site (eg, cleft lip, cleft palate, clubfoot) or be part of a syndrome of multiple. (msdmanuals.com)
Coronavirus6
- ABSTRACT A literature review of publically available information was undertaken to summarize current understanding and gaps in knowledge about Middle East respiratory syndrome coronavirus (MERS-CoV), including its origin, transmission, effective control measures and management. (who.int)
- RÉSUMÉ Une analyse documentaire des informations publiques disponibles a été entreprise afin de passer en revue les connaissances et les lacunes actuelles sur le coronavirus du syndrome respiratoire du Moyen-Orient (MERS-CoV), notamment sur son origine, la transmission, les mesures de lutte efficaces et la prise en charge. (who.int)
- Identification of a novel coronavirus in patients with severe acute respiratory syndrome. (cdc.gov)
- A novel coronavirus associated with severe acute respiratory syndrome. (cdc.gov)
- Coronavirus as a possible cause of severe acute respiratory syndrome. (cdc.gov)
- Cases of severe acute respiratory syndrome (SARS) were investigated for SARS coronavirus (SARS-CoV) through RNA tests, serologic response, and viral culture. (cdc.gov)
Disease4
- The white-nose syndrome is a disease that is caused by the fungus, P. destructans, it grows on the bats' skin. (fviss.ca)
- Although Alzheimer disease (AD) is more frequent in individuals with Down syndrome (DS), the main contributing factor is unknown. (medscape.com)
- It is important to obtain an accurate and thorough history of medications and recent ingestions so that the symptoms of this syndrome can be distinguished from those of other disease processes that present similarly. (medscape.com)
- In early 2003, severe acute respiratory syndrome (SARS) was recognized as a newly emerging pneumonic disease ( 1 - 3 ). (cdc.gov)
Fraser's2
- Fraser's syndrome. (medscape.com)
- Cryptophthalmos is often associated with Fraser's syndrome. (bvsalud.org)
Imposter1
- I suffer from imposter syndrome, so yes, I definitely felt uncertain. (sfu.ca)
Respiratory syndrome10
- Role of China in the quest to define and control severe acute respiratory syndrome. (cdc.gov)
- Outbreak of severe acute respiratory syndrome - worldwide, 2003. (cdc.gov)
- Severe acute respiratory syndrome - Singapore, 2003. (cdc.gov)
- Update: severe acute respiratory syndrome - Toronto, Canada, 2003. (cdc.gov)
- Outbreak of severe acute respiratory syndrome in Hong Kong Special Administrative Region: case report. (cdc.gov)
- A major outbreak of severe acute respiratory syndrome in Hong Kong. (cdc.gov)
- Transmission dynamics and control of severe acute respiratory syndrome. (cdc.gov)
- Effectiveness of precautions against droplets and contact in prevention of nosocomial transmission of severe acute respiratory syndrome (SARS). (cdc.gov)
- Investigation of a nosocomial outbreak of severe acute respiratory syndrome (SARS) in Toronto, Canada. (cdc.gov)
- Cumulative number of reported probable cases of severe acute respiratory syndrome (SARS). (cdc.gov)
Affects5
- What affects the larynx of babies with Fraser syndrome? (curvesandchaos.com)
- White-nose syndrome affects all life stages of hibernating bats. (fviss.ca)
- Researchers estimate that BOR/BO syndrome affects about 1 in 40,000 people. (medlineplus.gov)
- Androgen insensitivity syndrome is a condition that affects sexual development before birth and during puberty. (nipt-geneplanet.com)
- Angelman syndrome affects the nervous system. (nipt-geneplanet.com)
19861
- Koenig and Spranger (1986) noted that eye lesions are apparently nonobligatory components of the syndrome. (wikipedia.org)
20182
20223
- In a 2022 case study , researchers presented a case of visual snow syndrome developing after LASIK surgery . (healthline.com)
- Another 2022 case study reported visual snow syndrome in a person who experienced a series of mild concussions . (healthline.com)
- Another 2022 case study reported probable visual snow syndrome related to methylphenidate to treat a child with attention deficit hyperactivity disorder (ADHD) . (healthline.com)
Symptoms of this syndr1
- The signs and symptoms of this syndrome are present from birth or become apparent in early childhood. (nipt-geneplanet.com)
Karyotype1
- In patients with abnormal karyotype ( n = 3), 1 had trisomy 18 (47,XX) and died after 3 months and 2 had different types of mosaic Turner syndrome. (who.int)
Abbotsford2
- The Fraser Valley Down Syndrome Society (FVDSS) is a parent-run support group based in Abbotsford, B.C. for families of persons with Down syndrome in the Langley to Hope areas (including Pitt Meadows and Maple Ridge). (fvdss.org)
- The Fraser Valley Child Development Centre provides services that enhance the quality of life for children and youth with diverse abilities and their families throughout the Fraser Valley region, including Abbotsford, Mission, Chilliwack, and Fraser Cascades. (fvcdc.org)
Severe1
- About 25% of people with visual snow syndrome have severe depression or anxiety . (healthline.com)
Disorder1
- Visual snow syndrome is a recently discovered neurological disorder that received its name in 2013 . (healthline.com)
Siblings1
- These links will lead to online support groups for parents, caretakers, siblings, and survivors of Shaken Baby Syndrome. (dontshake.org)