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Results 1 - 8 of 8 for Aarskog syndrome
  1. Aarskog-Scott syndrome 
    ... 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-Scott syndrome National Organization for Rare Disorders ( ...
    https://medlineplus.gov/genetics/condition/aarskog-scott-syndrome - Genetics
  2. FGD1 gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/fgd1 - Genetics
  3. 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
  4. 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 ...
    https://medlineplus.gov/cleftlipandpalate.html - Health Topics
  5. 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 ...
    https://medlineplus.gov/congenitalheartdefects.html - Health Topics
  6. 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
  7. Short stature, hyperextensibility, hernia, ocular depression, Rieger anomaly, and teething delay 
    ... 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 ...
    https://medlineplus.gov/...ression-rieger-anomaly-and-teething-delay - Genetics
  8. PIK3R1 gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/pik3r1 - Genetics