Catalog

Congenital myopathy with no specific features or minimal change

No MMS code

Link to WHO Definition

Congenital myopathy with no specific features or minimal change – http://id.who.int/icd/entity/2094937414

Congenital muscular disorder characterised by non-specific myopathic changes, such as mild variation in fibre size, and slight abnormality in fibre type distribution. The abnormal muscle pathology is assumed to result from delayed muscle fibre growth and differentiation due to a probable defective neural influence upon the developing muscles.