NEUROPATHY IN FAMILIAL AMYLOIDOSIS, FINNISH TYPE (FAF) - ELECTROPHYSIOLOGICAL STUDIES

被引:34
作者
KIURU, S
SEPPALAINEN, AM
机构
[1] Department of Neurology, University of Helsinki, Helsinki
关键词
FAMILIAL AMYLOIDOSIS; FINNISH TYPE; GELSOLIN; POLYNEUROPATHY; FACIAL NERVE PALSY; CARPAL TUNNEL SYNDROME;
D O I
10.1002/mus.880170307
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We report, for the fi rst time, electrophysiological findings in the Finnish type of familial amyloidosis (FAF), a gelsolin-related form of systemic amyloidosis. Electromyography, nerve conduction studies, and blink reflex examinations were performed in 30 patients (age range 27-74 years). Cranial nerve involvement was detected in all, and peripheral nerve involvement in the majority of patients. Carpal tunnel syndrome was a characteristic feature of FAF, previously unrecognized. Myokymia-type short spontaneous bursts in frontal muscles were found in 3 younger patients. In addition to signs of axonal degeneration we found slow nerve conduction, prolonged distal motor latencies, and conduction blocks suggestive of demyelination. Most nerve conduction velocities correlated remarkably with age. We conclude that FAF is characterized not only by distinct clinical and molecular biological features but also by electrophysiological findings, which enable differentiation from other hereditary amyloidoses. (C) 1994 John Wiley and Sons, Inc.
引用
收藏
页码:299 / 304
页数:6
相关论文
共 31 条
[2]   FAMILIAL AMYLOIDOSIS WITH CRANIAL NEUROPATHY AND CORNEAL LATTICE DYSTROPHY [J].
BOYSEN, G ;
GALASSI, G ;
KAMIENIECKA, Z ;
SCHLAEGER, J ;
TROJABORG, W .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1979, 42 (11) :1020-1030
[3]   GELSOLIN-DERIVED FAMILIAL AMYLOIDOSIS CAUSED BY ASPARAGINE OR TYROSINE SUBSTITUTION FOR ASPARTIC-ACID AT RESIDUE 187 [J].
DELACHAPELLE, A ;
TOLVANEN, R ;
BOYSEN, G ;
SANTAVY, J ;
BLEEKERWAGEMAKERS, L ;
MAURY, CPJ ;
KERE, J .
NATURE GENETICS, 1992, 2 (02) :157-160
[4]   FAMILIAL AMYLOIDOSIS, FINNISH TYPE - G654 -] A MUTATION OF THE GELSOLIN GENE IN FINNISH FAMILIES AND AN UNRELATED AMERICAN FAMILY [J].
DELACHAPELLE, A ;
KERE, J ;
SACK, GH ;
TOLVANEN, R ;
MAURY, CPJ .
GENOMICS, 1992, 13 (03) :898-901
[5]   DISSOCIATED SENSATION IN AMYLOIDOSIS - COMPOUND ACTION POTENTIAL QUANTITATIVE HISTOLOGIC AND TEASED-FIBER AND ELECTRON MICROSCOPIC STUDIES OF SURAL NERVE BIOPSIES [J].
DYCK, PJ ;
LAMBERT, EH .
ARCHIVES OF NEUROLOGY, 1969, 20 (05) :490-&
[6]   CALCIUM AND POLYPHOSPHOINOSITIDE CONTROL OF CYTOSKELETAL DYNAMICS [J].
FORSCHER, P .
TRENDS IN NEUROSCIENCES, 1989, 12 (11) :468-474
[7]   BETA-2-MICROGLOBULIN - A NEW FORM OF AMYLOID PROTEIN ASSOCIATED WITH CHRONIC-HEMODIALYSIS [J].
GEJYO, F ;
ODANI, S ;
YAMADA, T ;
HONMA, N ;
SAITO, H ;
SUZUKI, Y ;
NAKAGAWA, Y ;
KOBAYASHI, H ;
MARUYAMA, Y ;
HIRASAWA, Y ;
SUZUKI, M ;
ARAKAWA, M .
KIDNEY INTERNATIONAL, 1986, 30 (03) :385-390
[8]   GELSOLIN VARIANT (ASN-187) IN FAMILIAL AMYLOIDOSIS, FINNISH TYPE [J].
GHISO, J ;
HALTIA, M ;
PRELLI, F ;
NOVELLO, J ;
FRANGIONE, B .
BIOCHEMICAL JOURNAL, 1990, 272 (03) :827-830
[9]   AMYLOIDOSIS DUE TO A MUTATION OF THE GELSOLIN GENE IN AN AMERICAN FAMILY WITH LATTICE CORNEAL-DYSTROPHY TYPE-II [J].
GOREVIC, PD ;
MUNOZ, PC ;
GORGONE, G ;
PURCELL, JJ ;
RODRIGUES, M ;
GHISO, J ;
LEVY, E ;
HALTIA, M ;
FRANGIONE, B .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (25) :1780-1785
[10]  
HALTIA M, 1990, AM J PATHOL, V136, P1223