Hereditary Congenital Facial Paresis I: Hereditary Congenital Facial Paresis I is a very rare condition characterized by underdevelopment of the facial nerves (particularly sixth and seventh cranial nerves) which causes facial paralysis. It is linked to a genetic defect on chromosome 3q. The facial paralysis may affect one or both sides of the face. More detailed information about the symptoms, causes, and treatments of Hereditary Congenital Facial Paresis I is available below.
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Prognosis for Hereditary Congenital Facial Paresis I: The prognosis is usually good with most people adapting to the condition using various therapies. They can lead normal fulfilling lives.
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