서론=65,70,1
1. Clinical approach=65,70,2
2. Muscular dystrophy=66,71,1
2-(1). Duchenne/Becker muscular dystrophy (DMD/BMD)=66,71,2
2-(2) Limb-girdle muscular dystrophy (LGMD) 및 other type muscular dystrophy=67,72,1
2-(3) Congenital muscular dystrophy (CMD)=67,72,2
3. Congential Myopathy=68,73,1
4. Spinal Muscular Atrophy=68,73,1
5. Metabolic myopathy including mitochondiral myopathy=68,73,2
5-(1) Glycogen storage disease (GSD)=69,74,1
5-(2) mitochondrial myopathy=69,74,2
결론=70,75,1
Table 1. Major neuromuscular disorders in childhood=71,76,1
Table 2. Genetic classification of muscular dystrophy=71,76,1
Table 3. Antibodies routinely used in analysis of muscle biopsies=72,77,1
Table 4. Congenital muscular dystrophy: Clinical and genetic heterogeneity -Proposed classification -=72,77,1
Figure 1. Diagnostic flow in muscular dystrophy=73,78,1
Figure 2. The investigation of mitochondrial disorders=73,78,1