| Finnish type familial amyloid p. |
a slowly progressive form of familial amyloid polyneuropathy whose earliest symptom is usually lattice dystrophy of the cornea. Later developments include cranial nerve palsy, paresis along the upper branch of the facial nerve, and renal amyloidosis. Called also Meretoja type familial amyloid p. and Meretoja's syndrome.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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