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Fg Syndrome

Fg Syndrome Causes

FG syndrome is caused by a genetic mutation of the long arm (q) of the chromosome X12-X21.

Fg Syndrome Definition

FG syndrome is a rare genetic disorder that causes poor muscle tone, an abnormally large head, and recurring rectal problems.

Fg Syndrome Diagnosis

The diagnosis can be done by genetic testing.

Fg Syndrome Symptoms and Signs

The symptoms of the disease include seizures, hypotonia, brain abnormalities, a short stature, chronic constipation, and streaks of light and dark pigments on the skin.

Fg Syndrome Treatment

There is no exact treatment available for the disease. Those who are suffering from mental retardation may undergo special education programs.

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