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Aarskog-Scott syndrome (medical condition): A rare genetic condition characterized by facial, hand, genital and growth abnormalities.
See also:
Aarskog Syndrome:
»Introduction: Aarskog Syndrome
»Symptoms of Aarskog Syndrome
Aarskog-Scott syndrome: SYN: faciodigitogenital dysplasia.
Source: Stedman's Medical Spellchecker, © 2006 Lippincott Williams & Wilkins. All rights reserved.
Aarskog-Scott syndrome: Multiple limb and genital abnormalities with short stature, hypertelorism, downslanting palpebral fissures, anteverted nostrils joint laxity, shawl scrotum, and occasional mental retardation. The phenotype varies with age and postpuberal males have only minor remnant manifestations of the prepuberal phenotype.
Source: Diseases Database
These medical condition or symptom topics may be relevant to medical information for Aarskog-Scott syndrome:
Aarskog-Scott syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Aarskog-Scott syndrome, or a subtype of Aarskog-Scott syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when if affects 1 person per 2,000.
They list Aarskog-Scott syndrome as a "rare disease".
Source - Orphanet
Aarskog-Scott syndrome: Another name for Aarskog Syndrome (or close medical condition association).
»Introduction: Aarskog Syndrome
»Symptoms of Aarskog Syndrome
Some of the symptoms of Aarskog-Scott syndrome incude:
See full list of 40 symptoms of Aarskog-Scott syndrome (Aarskog Syndrome)
These medical disease topics may be related to Aarskog-Scott syndrome:
Source: Diseases Database
Source - NIH
Source: Diseases Database
Search to find out more about Aarskog-Scott syndrome:
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