Isolated hereditary congenital facial paralysis

Orpha code: 306527OMIM code: 601471

Definicja

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
Klasyfikacja

Morphological anomaly

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

No additional description.

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