Greig Cephalopolysyndactyly Syndrome: A rare genetic disorder characterized by premature closing of skull bones and craniofacial abnormalities, finger and toe abnormalities. More detailed information about the symptoms, causes, and treatments of Greig Cephalopolysyndactyly Syndrome is available below.
See full list of 32 symptoms of Greig Cephalopolysyndactyly Syndrome
Read more about complications of Greig Cephalopolysyndactyly Syndrome.
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See full list of 22 occasional symptoms of Greig Cephalopolysyndactyly Syndrome
Read more about causes of Greig Cephalopolysyndactyly Syndrome
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Prognosis for Greig Cephalopolysyndactyly Syndrome: The prognosis varies depending on the type and severity of symptoms that develop. Prompt diagnosis and appropriate treatment can improve prognosis and quality of life. Generally a good prognosis and a normal life expectancy can be expected. The main symptom of concern is the mild mental retardation that can occur in some patients.
More about prognosis of Greig Cephalopolysyndactyly Syndrome
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Greig Cephalopolysyndactyly Syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Greig Cephalopolysyndactyly Syndrome, or a subtype of Greig Cephalopolysyndactyly Syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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