Isolated hereditary congenital facial paralysis
MONDO:0011090Isolated 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.
Also known as: HCFP, MBS2 (formerly), Mobius syndrome 2 (formerly), Moebius syndrome 2 (formerly), facial palsy, congenital, unilateral or bilateral, facial paresis hereditary congenital, facial paresis, hereditary congenital, hereditary congenital facial paresis
2 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trials