Myopathy, Central Core

MeSH 搜索器

Myopathy, Central Core

An inherited congenital myopathic condition characterized by weakness and hypotonia in infancy and delayed motor development. Muscle biopsy reveals a condensation of myofibrils and myofibrillar material in the central portion of each muscle fiber. (Adams et al., Principles of Neurology, 6th ed, p1452)

推出的年份: 2000

树号: C05.651.575.300, C10.668.491.550.300

MeSH 单一 ID: D020512

进入的组:

Central Core Myopathies
Myopathies, Central Core
Shy-Magee Syndrome
Shy Magee Syndrome
Syndrome, Shy-Magee
Central Core Myopathy
Central Core Disease
Central Core Diseases
Central Core Disease of Muscle

早前的内容:

Muscles/enzymology (1963-1999)
Muscular Atrophy (1963-1999)

All MeSH Categories
- Diseases Category
  - Musculoskeletal Diseases [C05]
    - Muscular Diseases [C05.651]
      - Myopathies, Structural, Congenital [C05.651.575]

All MeSH Categories
- Diseases Category
  - Nervous System Diseases [C10]
    - Neuromuscular Diseases [C10.668]
      - Muscular Diseases [C10.668.491]
        
        Myopathies, Structural, Congenital [C10.668.491.550]
        
        Myopathies, Nemaline [C10.668.491.550.290]
        
        Myopathy, Central Core [C10.668.491.550.300]

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MeSH 搜索器

Myopathy, Central Core

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