Inherited neuromuscular disorders: Pathway to diagnosis

被引:15
作者
Menezes, Manoj P. [1 ]
North, Kathryn N. [1 ,2 ]
机构
[1] Childrens Hosp Westmead, Inst Neurosci & Muscle Res, Sydney, NSW 2145, Australia
[2] Univ Sydney, Discipline Paediat & Child Hlth, Fac Med, Sydney, NSW 2006, Australia
关键词
child; Duchenne; hypotonia; muscle weakness; muscular dystrophy; neuromuscular disease; MARIE-TOOTH DISEASE; FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY; CONGENITAL MYOPATHIES; ABNORMALITIES; HISTORY; ATROPHY; GENE; 1A;
D O I
10.1111/j.1440-1754.2011.02210.x
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Muscle weakness in childhood can be caused by a lesion at any point extending from the motor cortex, brainstem and spinal cord to the anterior horn cell, peripheral nerve, neuromuscular junction and muscle. A comprehensive history and physical examination is essential to aid classification of the neuromuscular disorder and direct gene testing. The more common disorders such as spinal muscular atrophy, Duchenne muscular dystrophy, myotonic dystrophy and facioscapulohumeral dystrophy may be diagnosed on direct gene testing based on the history and clinical examination. The congenital myopathies are classified based on structural abnormalities on muscle biopsy, while protein abnormalities on immunohistochemistry and immunoblotting aid classification of the muscular dystrophies. In this review, we provide an approach to diagnosis of a child with weakness, with a focus on the inherited neuromuscular disorders, and the features on history, examination and investigation that help to distinguish between them.
引用
收藏
页码:458 / 465
页数:8
相关论文
共 38 条
[1]  
Anthony DC, 2003, NEUROMUSCULAR DISORD, P75
[2]   Neuromuscular hip dysplasia in Charcot-Marie-Tooth disease type 1A [J].
Bamford, Nigel S. ;
White, Klane K. ;
Robinett, Stephanie A. ;
Otto, Randolph K. ;
Gospe, Sidney M., Jr. .
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2009, 51 (05) :408-411
[3]   Prevalence of structural cardiac abnormalities in patients with myotonic dystrophy type I [J].
Bhakta, D ;
Lowe, MR ;
Groh, WJ .
AMERICAN HEART JOURNAL, 2004, 147 (02) :224-227
[4]   Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication - Clinical and electrophysiological phenotype study and influencing disease severity in 119 cases [J].
Birouk, N ;
Gouider, R ;
LeGuern, E ;
Gugenheim, M ;
Tardieu, S ;
Maisonobe, T ;
LeForestier, N ;
Agid, Y ;
Brice, A ;
Bouche, P .
BRAIN, 1997, 120 :813-823
[5]   The Evaluation of the Hypotonic Infant [J].
Bodensteiner, John B. .
SEMINARS IN PEDIATRIC NEUROLOGY, 2008, 15 (01) :10-20
[6]   The genetic convergence of charcot-marie-tooth disease types 1 and 2 and the role of genetics in sporadic neuropathy [J].
Boerkoel C.F. ;
Takashima H. ;
Lupski J.R. .
Current Neurology and Neuroscience Reports, 2002, 2 (1) :70-77
[7]   Diagnosis and management of Duchenne muscular dystrophy, part 2: implementation of multidisciplinary care [J].
Bushby, Katharine ;
Finkel, Richard ;
Birnkrant, David J. ;
Case, Laura E. ;
Clemens, Paula R. ;
Cripe, Linda ;
Kaul, Ajay ;
Kinnett, Kathi ;
McDonald, Craig ;
Pandya, Shree ;
Poysky, James ;
Shapiro, Frederic ;
Tomezsko, Jean ;
Constantin, Carolyn .
LANCET NEUROLOGY, 2010, 9 (02) :177-189
[8]   Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management [J].
Bushby, Katharine ;
Finkel, Richard ;
Birnkrant, David J. ;
Case, Laura E. ;
Clemens, Paula R. ;
Cripe, Linda ;
Kaul, Ajay ;
Kinnett, Kathi ;
McDonald, Craig ;
Pandya, Shree ;
Poysky, James ;
Shapiro, Frederic ;
Tomezsko, Jean ;
Constantin, Carolyn .
LANCET NEUROLOGY, 2010, 9 (01) :77-93
[9]   Failure of early diagnosis in symptomatic Duchenne muscular dystrophy [J].
Bushby, KMD ;
Hill, A ;
Steele, JG .
LANCET, 1999, 353 (9152) :557-558
[10]   Intelligence and Duchenne muscular dystrophy: Full-scale, verbal, and performance intelligence quotients [J].
Cotton, S ;
Voudouris, NJ ;
Greenwood, KM .
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2001, 43 (07) :497-501