Cephalopolysyndactyly: A rare genetic disorder characterized by premature closing of skull bones and craniofacial abnormalities, finger and toe abnormalities. The type and severity of symptoms is variable with many cases remaining undiagnosed because their condition is relatively mild and doesn't cause many problems. More detailed information about the symptoms, causes, and treatments of Cephalopolysyndactyly is available below.
See full list of 19 symptoms of Cephalopolysyndactyly
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See full list of 14 occasional symptoms of Cephalopolysyndactyly
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Prognosis for Cephalopolysyndactyly: 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.
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Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Cephalopolysyndactyly as a "rare disease".
Source - Orphanet
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