UNIFORM SLOWING OF CONDUCTION VELOCITIES IN CHARCOT-MARIE-TOOTH POLYNEUROPATHY TYPE-1

被引:78
作者
KAKU, DA
PARRY, GJ
MALAMUT, R
LUPSKI, JR
GARCIA, CA
机构
[1] LOUISIANA STATE UNIV,SCH MED,DEPT NEUROL,1542 TULANE AVE,NEW ORLEANS,LA 70122
[2] BAYLOR COLL MED,INST MOLEC GENET,CTR HUMAN GENOME,HOUSTON,TX 77030
[3] BAYLOR COLL MED,DEPT PEDIAT,HOUSTON,TX 77030
关键词
D O I
10.1212/WNL.43.12.2664
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We evaluated motor conduction studies in 129 patients with Charcot-Marine-Tooth disease type 1 (CMT1) to assess the uniformity of conduction slowing within individual patients. Conduction velocities were nearly identical in proximal and distal nerve segments (r = 0.86), from side to side (r = 0.95), in ipsilateral median and ulnar nerves (r = 0.94), and even in the median and peroneal nerves (r = 0.70). Segmental amplitude reductions suggestive of possible conduction block or differential dispersion were present in only 19 of 360 nerve segments studied (5.3%), and interphase cancellation or focal compression were likely alternative explanations in these cases. These findings support the concept that uniform conduction slowing characterizes CMT1, in distinction to acquired demyelinating polyneuropathies, which feature multifocal conduction abnormalities. We conclude that normal nerve conduction velocity in a single motor nerve can reliably exclude CMT1, but evaluation of several nerves and nerve segments to establish uniformity of conduction slowing is important in making this diagnosis. The homogeneity of the disturbance of nerve conduction favors a primary Schwann-cell disorder as the basis of CMT1.
引用
收藏
页码:2664 / 2667
页数:4
相关论文
共 28 条
[1]   THE APPLICATION OF NERVE-CONDUCTION AND CLINICAL-STUDIES TO GENETIC-COUNSELING IN HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE-I [J].
BERCIANO, J ;
COMBARROS, O ;
CALLEJA, J ;
POLO, JM ;
LENO, C .
MUSCLE & NERVE, 1989, 12 (04) :302-306
[2]   CONDUCTION BLOCK IN CLINICAL-PRACTICE [J].
CORNBLATH, DR ;
SUMNER, AJ ;
DAUBE, J ;
GILLIAT, RW ;
BROWN, WF ;
PARRY, GJ ;
ALBERS, JW ;
MILLER, RG ;
PETAJAN, J .
MUSCLE & NERVE, 1991, 14 (09) :869-871
[3]   GENETIC-LINKAGE OF HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE-I (CHARCOT-MARIE-TOOTH DISEASE) TO MARKERS OF CHROMOSOME-1 AND CHROMOSOME-17 [J].
DEFESCHE, JC ;
HOOGENDIJK, JE ;
DEVISSER, M ;
DEVISSER, BWO ;
BOLHUIS, PA .
NEUROLOGY, 1990, 40 (09) :1450-1453
[4]  
Dyck P.J., 1984, PERIPHERAL NEUROPATH, P1600
[5]   LOWER MOTOR AND PRIMARY SENSORY NEURON DISEASES WITH PERONEAL MUSCULAR ATROPHY .I. NEUROLOGIC GENETIC AND ELECTROPHYSIOLOGIC FINDINGS IN HEREDITARY POLYNEUROPATHIES [J].
DYCK, PJ ;
LAMBERT, EH .
ARCHIVES OF NEUROLOGY, 1968, 18 (06) :603-+
[6]   LONGITUDINAL-STUDY OF NEUROPATHIC DEFICITS AND NERVE-CONDUCTION ABNORMALITIES IN HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE-1 [J].
DYCK, PJ ;
KARNES, JL ;
LAMBERT, EH .
NEUROLOGY, 1989, 39 (10) :1302-1308
[7]   EVOLUTION OF NERVE-CONDUCTION ABNORMALITIES IN CHILDREN WITH DOMINANT HYPERTROPHIC NEUROPATHY OF THE CHARCOT-MARIE-TOOTH TYPE [J].
GUTMANN, L ;
FAKADEJ, A ;
RIGGS, JE .
MUSCLE & NERVE, 1983, 6 (07) :515-519
[8]   THE CLINICAL-FEATURES OF HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE-I AND TYPE-II [J].
HARDING, AE ;
THOMAS, PK .
BRAIN, 1980, 103 (JUN) :259-280
[9]  
HOOGENDIJK JE, 1992, MUSCLE NERVE, V15, P520
[10]   NERVE-CONDUCTION STUDIES IN CHARCOT-MARIE-TOOTH POLYNEUROPATHY ASSOCIATED WITH A SEGMENTAL DUPLICATION OF CHROMOSOME-17 [J].
KAKU, DA ;
PARRY, GJ ;
MALAMUT, R ;
LUPSKI, JR ;
GARCIA, CA .
NEUROLOGY, 1993, 43 (09) :1806-1808