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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 ...
- 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).
- ... 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 ...
- 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 ...
- 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 ...
- ... 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- ...
- ... 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 ...
- ... 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 ...
- ... 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 ...
- ... 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 ...