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Congenital myopathy : ウィキペディア英語版
Congenital myopathy

Congenital myopathy is a very broad term for any muscle disorder present at birth. This defect primarily affects skeletal muscle fibres and causes muscular weakness and/or hypotonia. Congenital myopathies account for one of the top neuromuscular disorders in the world today, comprising approximately 6 in 100,000 live births every year. As a whole, congenital myopathies can be broadly classified as follows:
*A distinctive abnormality in skeletal muscle fibres on the cellular level; observable via light microscope
*Symptoms of muscle weakness and hypotonia
*Is a congenital disorder, meaning it occurs during development and symptoms present themselves at birth or in early life.
*Is a genetic disorder.
==Classification of congenital myopathies==


抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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