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Results 1 - 10 of 136 for SCOTT SYNDROME
  1. Aarskog-Scott syndrome 
    Aarskog-Scott syndrome is a genetic disorder that affects the development of many parts of the body, most commonly the head and face, the hands and feet, and ...
    https://medlineplus.gov/genetics/condition/aarskog-scott-syndrome - Genetics
  2. Aarskog syndrome 
    Aarskog syndrome is a very rare disease that affects a person's height, muscles, skeleton, genitals, and appearance. It can be passed down through families (inherited).
    https://medlineplus.gov/ency/article/001654.htm - Medical Encyclopedia
  3. FGD1 gene 
    ... FGD1 gene have been found to cause Aarskog-Scott syndrome, a rare condition that occurs primarily in males. ... of abnormalities that occur in people with Aarskog-Scott syndrome. More About This Health Condition AAS faciogenital dysplasia ...
    https://medlineplus.gov/genetics/gene/fgd1 - Genetics
  4. Learning Disabilities (National Library of Medicine)  
    What is a learning disability? Learning disabilities are conditions that affect the ability to learn. They can cause problems with: Understanding what ...
    https://medlineplus.gov/learningdisabilities.html - Health Topics
  5. Craniofacial Abnormalities (National Library of Medicine)  
    Craniofacial is a medical term that relates to the bones of the skull and face. Craniofacial abnormalities are birth defects of the face or head. Some, like cleft ...
    https://medlineplus.gov/craniofacialabnormalities.html - Health Topics
  6. Wagner syndrome 
    ... on PubMed Meredith SP, Richards AJ, Flanagan DW, Scott JD, Poulson AV, Snead MP. Clinical characterisation and molecular analysis of Wagner syndrome. Br J Ophthalmol. 2007 May;91(5):655- ...
    https://medlineplus.gov/genetics/condition/wagner-syndrome - Genetics
  7. COL2A1 gene 
    ... Yates JR, Lane C, Nicol M, Harper PS, Scott JD, Snead MP. Variation in the vitreous phenotype of Stickler syndrome can be caused by different amino acid substitutions ...
    https://medlineplus.gov/genetics/gene/col2a1 - Genetics
  8. Neurodevelopmental disorder with or without anomalies of the brain, eye, or heart 
    ... van Gassen KLI, van Binsbergen E, Barkovich AJ, Scott DA, Sherr EH. De Novo Mutations of RERE Cause a Genetic Syndrome with Features that Overlap Those Associated with Proximal ...
    https://medlineplus.gov/...thout-anomalies-of-the-brain-eye-or-heart - Genetics
  9. RERE gene 
    ... van Gassen KLI, van Binsbergen E, Barkovich AJ, Scott DA, Sherr EH. De Novo Mutations of RERE Cause a Genetic Syndrome with Features that Overlap Those Associated with Proximal ...
    https://medlineplus.gov/genetics/gene/rere - Genetics
  10. SLC26A4 gene 
    ... ng0398-215. No abstract available. Citation on PubMed Scott DA, Wang R, Kreman TM, Sheffield VC, Karniski LP. The Pendred syndrome gene encodes a chloride-iodide transport protein. Nat ...
    https://medlineplus.gov/genetics/gene/slc26a4 - Genetics
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