Magnetic resonance imaging of muscle in nemaline myopathy

被引:79
作者
Jungbluth, H
Sewry, CA
Counsell, S
Allsop, J
Chattopadhyay, A
Mercuri, E
North, K
Laing, N
Bydder, G
Pelin, K
Wallgren-Pettersson, C
Muntoni, F
机构
[1] Guys Hosp, Dept Paediat Neurol, London SE1 9RT, England
[2] Hammersmith Hosp, Imperial Coll, Dubowitz Neuromuscular Ctr, London W12 0NN, England
[3] Robert Jones & Agnes Hunt Orthopaed Hosp, Dept Histopathol, Oswestry SY10 7AG, Shrops, England
[4] Hammersmith Hosp, Imperial Coll, Robert Steiner MRI Unit, London, England
[5] Childrens Hosp Westmead, Inst Neuromuscular Res, Sydney, NSW, Australia
[6] Univ Western Australia, Ctr Neuromuscular Disorders, Australian Neuromuscular Res Inst, Nedlands, WA 6009, Australia
[7] Univ Western Australia, Western Australian Inst Med Res, QEII Med Ctr, Med Res Ctr, Nedlands, WA 6009, Australia
[8] Univ Helsinki, Dept Med Genet, Helsinki, Finland
[9] Folkhalsan Dept Med Genet, Helsinki, Finland
关键词
nemaline (rod) myopathy; NEB gene; ACTA1; gene; muscle MRI; selective muscle involvement;
D O I
10.1016/j.nmd.2004.08.005
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We report muscle MRI findings of 10 patients from 8 families with nemaline myopathy. Patients with involvement of the nebulin (NEB) gene showed a consistent pattern of selective muscle involvement corresponding to clinical severity. In mild cases. there was complete sparing of thigh muscles and selective involvement of tibialis anterior and soleus. In moderate cases, there was predominant involvement of rectus femoris. vastus lateralis and hamstring muscles and diffuse involvement of anterior compartment and soleus. Patients with nemaline myopathy secondary to mutations in the skeletal muscle alpha-actin (ACTA1) gene showed diffuse involvement of thigh and leg muscles with relative sparing of the gastrocnemii. Selective muscle involvement in both genetic categories was distinct from what has been reported in other congenital myopathies We conclude that muscle MRI may be applied to distinguish nemaline myopathy from other conditions with similar clinical and histopathological features, to supplement clinical assessment in individual patients and to help direct genetic testing. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:779 / 784
页数:6
相关论文
共 26 条
[1]   CONGENITAL NONPROGRESSIVE MYOPATHY - CENTRAL CORE DISEASE AND NEMALINE MYOPTAHY IN 1 FAMILY [J].
AFIFI, AK ;
SMITH, JW ;
ZELLWEGER, H .
NEUROLOGY, 1965, 15 (04) :371-+
[2]   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
[3]   Mutations in the β-tropomyosin (TPM2) gene -: a rare cause of nemaline myopathy [J].
Donner, K ;
Ollikainen, M ;
Ridanpää, M ;
Christen, HJ ;
Goebel, HH ;
de Visser, M ;
Pelin, K ;
Wallgren-Pettersson, C .
NEUROMUSCULAR DISORDERS, 2002, 12 (02) :151-158
[4]   MR IMAGING OF FAT [J].
DOOMS, GC ;
HRICAK, H ;
MARGULIS, AR ;
DEGEER, G .
RADIOLOGY, 1986, 158 (01) :51-54
[5]   Mutations of the selenoprotein N gene, which is implicated in rigid spine muscular dystrophy, cause the classical phenotype of multiminicore disease:: Reassessing the nosology of early-onset myopathies [J].
Ferreiro, A ;
Quijano-Roy, S ;
Pichereau, C ;
Moghadaszadeh, B ;
Goemans, N ;
Bönnemann, C ;
Jungbluth, H ;
Straub, V ;
Villanova, M ;
Leroy, JP ;
Romero, NB ;
Martin, JJ ;
Muntoni, F ;
Voit, T ;
Estournet, B ;
Richard, P ;
Fardeau, M ;
Guicheney, P .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) :739-749
[6]   Nemaline myopathy caused by mutations in the muscle α-skeletal-actin gene [J].
Ilkovski, B ;
Cooper, ST ;
Nowak, K ;
Ryan, MM ;
Yang, N ;
Schnell, C ;
Durling, HJ ;
Roddick, LG ;
Wilkinson, I ;
Kornberg, AJ ;
Collins, KJ ;
Wallace, G ;
Gunning, P ;
Hardeman, EC ;
Laing, NG ;
North, KN .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (06) :1333-1343
[7]   A novel nemaline myopathy in the Amish caused by a mutation in troponin T1. [J].
Johnston, JJ ;
Kelley, RI ;
Crawford, TO ;
Morton, DH ;
Agarwala, R ;
Koch, T ;
Schäffer, AA ;
Francomano, CA ;
Biesecker, LG .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) :54-54
[8]   Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores [J].
Jungbluth, H ;
Müller, CR ;
Halliger-Keller, B ;
Brockington, M ;
Brown, SC ;
Feng, L ;
Chattopadhyay, A ;
Mercuri, E ;
Manzur, AY ;
Ferreiro, A ;
Laing, NG ;
Davis, MR ;
Roper, HP ;
Dubowitz, V ;
Bydder, G ;
Sewry, CA ;
Muntoni, F .
NEUROLOGY, 2002, 59 (02) :284-287
[9]   Mild phenotype of nemaline myopathy with sleep hypoventilation due to a mutation in the skeletal muscle α-actin (ACTA1) gene [J].
Jungbluth, H ;
Sewry, CA ;
Brown, SC ;
Nowak, KJ ;
Laing, NG ;
Wallgren-Pettersson, C ;
Pelin, K ;
Manzur, AY ;
Mercuri, E ;
Dubowitz, V ;
Muntoni, F .
NEUROMUSCULAR DISORDERS, 2001, 11 (01) :35-40
[10]  
JUNGBLUTH H, UNPUB MAGNETIC RESON