Subclinical semitendinosus and obturator externus involvement defines an autosomal dominant myopathy with early respiratory failure

被引:14
作者
Birchall, D
von der Hagen, M
Bates, D
Bushby, KMD
Chinnery, PF
机构
[1] Reg Neurosci Ctr, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
[2] Univ Newcastle Upon Tyne, Inst Human Genet, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
关键词
inclusion body myopathy; distal myopathy; magnetic resonance imaging; semitendinosus;
D O I
10.1016/j.nmd.2005.05.002
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We recently described a dominant limb myopathy characterised by early respiratory failure whilst affected individuals were still ambulant (autosomal dominant myopathy with early respiratory failure). Early diagnosis and exclusion of this disorder is difficult because of the insidious onset in late adult life and the highly selective muscle involvement, both clinically and pathologically. We performed muscle magnetic resonance imaging on seven cases of autosomal dominant myopathy with early respiratory failure (age range 37-66 years, 4 male) and show selective early involvement of semitendinosus and obturator externus on magnetic resonance imaging that cannot be detected clinically, with different rates of progression in closely related muscles. These findings are specific to autosomal dominant myopathy with early respiratory failure and enable early non-invasive diagnosis for individuals at risk. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:595 / 600
页数:6
相关论文
共 22 条
[1]   DISTRIBUTION OF MUSCLE DEGENERATION IN WELANDER DISTAL MYOPATHY - A MAGNETIC-RESONANCE-IMAGING AND MUSCLE BIOPSY STUDY [J].
AHLBERG, G ;
JAKOBSSON, F ;
FRANSSON, A ;
MORITZ, A ;
BORG, K ;
EDSTROM, L .
NEUROMUSCULAR DISORDERS, 1994, 4 (01) :55-62
[2]   A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B [J].
Bashir, R ;
Britton, S ;
Strachan, T ;
Keers, S ;
Vafiadaki, E ;
Lako, M ;
Richard, I ;
Marchand, S ;
Bourg, N ;
Argov, Z ;
Sadeh, M ;
Mahjneh, I ;
Marconi, G ;
Passos-Bueno, MR ;
Moreira, ED ;
Zatz, M ;
Beckmann, JS ;
Bushby, K .
NATURE GENETICS, 1998, 20 (01) :37-42
[3]  
CHAPON F, 1989, REV NEUROL, V145, P460
[4]   A novel autosomal dominant distal myopathy with early respiratory failure: Clinico-pathologic characteristics and exclusion of linkage to candidate genetic loci [J].
Chinnery, PF ;
Johnson, MA ;
Walls, TJ ;
Gibson, GJ ;
Fawcett, PRW ;
Jamieson, S ;
Fulthorpe, JJ ;
Cullen, M ;
Hudgson, P ;
Bushby, KMD .
ANNALS OF NEUROLOGY, 2001, 49 (04) :443-452
[5]   MYOPATHY WITH RESPIRATORY-FAILURE AND TYPICAL MYOFIBRILLAR LESIONS [J].
EDSTROM, L ;
THORNELL, LE ;
ALBO, J ;
LANDIN, S ;
SAMUELSSON, M .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1990, 96 (2-3) :211-228
[6]   CYTOPLASMIC BODY NEURO-MYOPATHY PRESENTING AS RESPIRATORY-FAILURE AND WEIGHT-LOSS [J].
JERUSALEM, F ;
LUDIN, H ;
BISCHOFF, A ;
HARTMANN, G .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1979, 41 (01) :1-9
[7]   NEMALINE MYOPATHY REPORT OF 4 CASES AND REVIEW OF LITERATURE [J].
KUITUNEN, P ;
NOPONEN, AL ;
DONNER, M ;
RAPOLA, J .
ACTA PAEDIATRICA SCANDINAVICA, 1972, 61 (03) :353-&
[9]   Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy [J].
Liu, J ;
Aoki, M ;
Illa, I ;
Wu, CY ;
Fardeau, M ;
Angelini, C ;
Serrano, C ;
Urtizberea, JA ;
Hentati, F ;
Ben Hamida, M ;
Bohlega, S ;
Culper, EJ ;
Amato, AA ;
Bossie, K ;
Oeltjen, T ;
Bejaoui, K ;
McKenna-Yasek, D ;
Hosler, BA ;
Schurr, E ;
Arahata, K ;
de Jong, PJ ;
Brown, RH .
NATURE GENETICS, 1998, 20 (01) :31-36
[10]   Muscle magnetic resonance imaging shows distinct diagnostic patterns in Welander and tibial muscular dystrophy [J].
Mahjneh, I ;
Lamminen, AE ;
Udd, B ;
Paetau, AE ;
Hackman, P ;
Korhola, OA ;
Somer, HVK .
ACTA NEUROLOGICA SCANDINAVICA, 2004, 110 (02) :87-93