Aarskog Syndrome

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Aarskog syndrome is a genetic disorder that extreme but rare. Patients with dwarf stature but the symptoms are not apparent until the child is three years, the face is not normal, musculoskeletal and genital abnormalities, and mentally disturbed. The disorder is associated with chromosome X. The name of this disease that is taken from its discoverer, Dagfinn Aarskog, pediatricians Norway, in 1970.

Signs and Symptoms: Front abnormal, musculoskeletal and genital abnormalities, and mentally disturbed.

Medical care that can be done is with surgery to correct some abnormalities.

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Posted on October 31, 2011 at 12:13 am by Health Medic · Permalink
In: Children Disease, Syndrome · Tagged with: , ,

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