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... Aarskog syndrome is an inherited disease characterized by short stature , facial abnormalities, musculoskeletal, and genital anomalies.
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Aarskog-Scott syndrome - Wikipedia, the free encyclopedia
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Aarskog syndrome - Overview, Aarskog syndrome is an inherited disease that affe... ... Aarskog syndrome is an inherited disease that affects a person's height, muscles, skeleton, genitals, and appearance of the face. Inherited means that it is passed down through families...
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Aarskog syndrome is a genetic disorder that is linked to the X chromosome. It affects mainly males, but females may have a milder form. The condition is caused by changes (mutations) in a gene called "faciogenital dysplasia" (FGDY1)
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Aarskog Syndrome falls under the rare disorder category. It is very rare genetic abnormality which causes various distortions in the physical and mental frame of the human being. It is not noticeable on most people until they reach the age of three.
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The Aarskog Syndrome Parents Support Group's purpose is to educate the public about the features and possible delays or learning difficulties that may or may not effect some of children with Aarskog Syndrome and to offer support by mail or phone when needed.
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Aarskog syndrome Information from Drugs.com ... Aarskog syndrome is an inherited disease that affects a person's height, muscles, skeleton, genitals, and appearance of the face. Inherited means that it is passed down through families.
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Aarskog Syndrome information center covers causes, prevention, symptoms, diagnosis, treatment, incidence, risk factors, signs, tests, support groups, complications, and prognosis. ... Aarskog syndrome is an inherited disease characterized by short stature, facial abnormalities, musculoskeletal, and genital anomalies.
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