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Aarskog syndrome Health Article
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Definition
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.
Causes, incidence, and risk factors
Aarskog syndrome is a genetic disorder. 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).
Symptoms
Signs and tests
Treatment
Moving the teeth (orthodontic treatment) may be done for some of the abnormal facial features.
Support Groups
The MAGIC Foundation for Children's Growth is a support group for Aarskog syndrome and can be found at www.magicfoundation.org.
Expectations (prognosis)
Some people may have mild degrees of mental slowness, but affected children usually have good social skills. Some males may have problems with fertility.
Complications
Calling your health care provider
Call your health care provider if your child has delayed growth or if you notice any of the symptoms described here. Seek genetic counseling if there is a history of Aarskog syndrome in your family. Contact a genetic specialist if your doctor thinks you or your child may have Aarskog syndrome. |
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