Isolated hereditary congenital facial paralysis

Orpha code: 306527OMIM code: 601471

Definition

Isolated hereditary congenital facial paralysis (IHCFP) is an extremely rare neurological disorder presumed to result from maldevelopment of the facial nucleus and/or cranial nerve and has been reported in fewer than 10 families to date. It manifests as non-progressive, isolated, unilateral or bilateral, symmetrical or asymmetrical facial palsy. Involvement of the branches of the facial nerve can be unequal.

Disease data
Classification

Morphological anomaly

ORPHA code
306527
OMIM code
601471
ICD10 code
Q87.0
ICD11 code
-

No additional description.

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