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Results 1 - 10 of 11 for Aarskog syndrome
  1. Aarskog syndrome is a very rare disease that affects a person's height, muscles, skeleton, genitals, and appearance. It ... Aarskog syndrome is a genetic disorder that is linked to the X chromosome. It affects mainly males, but ...
  2. ... not show signs and symptoms of the condition. Aarskog syndrome AAS Facio-digito-genital dysplasia Faciodigitogenital syndrome Faciogenital dysplasia FGDY Genetic Testing Registry: Aarskog syndrome Aarskog syndrome Disease InfoSearch National Organization for Rare ...
  3. ... formation and skeletal defects in faciogenital dysplasia (FGDY; Aarskog syndrome). Dev Dyn. 2000 Aug;218(4):573-86. ... Sorrentino V. Phenotypic and molecular characterisation of the Aarskog-Scott syndrome: a survey of the clinical variability in light ...
  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 ...
  5. ... associated with other conditions such as Down syndrome, Aarskog syndrome or fetal alcohol syndrome.
  6. ... person's mental and physical growth, including: Down syndrome Aarskog syndrome Cohen syndrome Fetal alcohol syndrome Trisomy 13 Rubella ...
  7. Cleft Lip and Palate (National Library of Medicine)  
    Cleft lip and cleft palate are birth defects that occur when a baby's lip or mouth do not form properly. They happen early during pregnancy. A baby can have ...
  8. Congenital Heart Defects (National Library of Medicine)  
    What are congenital heart defects? Congenital heart defects (CHDs) are problems with the structure of the heart. "Congenital" means that that the problems ...
  9. 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 ...
  10. ... Konig R, Haldorsen I, Johansson B, Woo JR, Aarskog D, Sagen JV, Kahn CR, Molven A, Njolstad PR. SHORT syndrome with partial lipodystrophy due to impaired phosphatidylinositol 3 ...
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