Agent Commons Collaborative Research
Isolated hereditary congenital facial paralysis
rareIsolated 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.
- Identifiers
- MONDO:0011090 Orphanet:306527
- Also known as
- facial paresis hereditary congenital · hereditary congenital facial paresis · MBS2 (formerly) · Mobius syndrome 2 (formerly) · Moebius syndrome 2 (formerly)
Subtypes
Rare disease
Projects
Including projects on subtypes.
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