CONGENITAL MYOPATHY AND CARDIOMYOPATHY WITH IDENTICAL ULTRASTRUCTURAL-CHANGES

被引:5
作者
DAVIS, DG
NELSON, KR
MARKESBERY, WR
机构
[1] UNIV KENTUCKY,ALBERT B CHANDLER MED CTR,DEPT NEUROL,LEXINGTON,KY 40536
[2] UNIV KENTUCKY,ALBERT B CHANDLER MED CTR,SANDERS BROWN CTR AGING,LEXINGTON,KY 40536
关键词
D O I
10.1001/archneur.1990.00530100111026
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
A 7-day-old girl with congenital hypotonia and unexplained episodes of bradycardia had a broad spectrum of similar skeletal muscle and myocardial degenerative ultrastructural abnormalities. Ultrastructural studies showed obliteration of cross striations, myofilament disorganization, streaming, smearing, clumping, and zigzag Z-band deformities. A decrease in glycogen, mitochondria, and T-tubular system occurred in the regions showing Z-band abnormalities of both skeletal muscle and myocardium. Concurrent structural cardiomyopathy should be considered in patients with congenital myopathies, particularly with unexplained cardiac conduction abnormalities or contractile insufficiency. Ultrastructural evaluation of skeletal and cardiac muscle may be necessary to define such disorders. © 1990, American Medical Association. All rights reserved.
引用
收藏
页码:1141 / 1144
页数:4
相关论文
共 18 条
[1]  
ASHFAQ S, 1987, MEDICINE, V66, P389
[2]  
BENDER AN, 1979, HDB CLIN NEUROLOGY, P16
[3]   LEUKOENCEPHALOPATHY IN OCULOCRANIOSOMATIC NEUROMUSCULAR DISEASE WITH RAGGED-RED FIBERS - MITOCHONDRIAL ABNORMALITIES DEMONSTRATED BY COMPUTERIZED TOMOGRAPHY [J].
BERTORINI, T ;
ENGEL, WK ;
DICHIRO, G ;
DALAKAS, M .
ARCHIVES OF NEUROLOGY, 1978, 35 (10) :643-647
[4]   COMMON ORIGIN OF RODS, CORES, MINIATURE CORES, AND FOCAL LOSS OF CROSS-STRIATIONS [J].
BETHLEM, J ;
ARTS, WF ;
DINGEMANS, KP .
ARCHIVES OF NEUROLOGY, 1978, 35 (09) :555-566
[5]  
FISHER ER, 1969, AM J CLIN PATHOL, V51, P619
[6]  
GARANCIS JC, 1970, LAB INVEST, V22, P468
[7]  
HOTCHI TI, 1975, SHIKOKU ACTA MEDICA, V31, P295
[8]  
KARPATI G, 1979, NEUROLOGY, V19, P553
[9]  
Landing B H, 1983, Pediatr Pathol, V1, P137
[10]  
MEIER C, 1983, NEW ENGL J MED, V308, P1536