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Aarskog syndrome

Introduction: Aarskog syndrome



Description of Aarskog syndrome

Aarskog 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 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

Aarskog syndrome: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Aarskog 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 syndrome, or a subtype of Aarskog syndrome, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Aarskog syndrome as a Disease

Aarskog syndrome (medical condition): See Aarskog Syndrome (disease information).
  »Introduction: Aarskog Syndrome
  »Symptoms of Aarskog Syndrome

More information on medical condition: Aarskog Syndrome:

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Source: Diseases Database

Source - NIH

External links related to: Aarskog syndrome

Source: Diseases Database

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