ICD-11 classes
08 Diseases of the nervous system
Diseases of neuromuscular junction or muscle
Primary disorders of muscles
8C70 — Muscular dystrophy
8C70.4 — Limb-girdle muscular dystrophy
8C70.41 — Recessive limb-girdle muscular dystrophy
ICD-11 8C70.41 — Recessive limb-girdle muscular dystrophy
Autosomal recessive limb girdle muscular dystrophies (LGMD2) are a group of genetically heterogeneous diseases that are typically characterised by progressive weakness and wasting of the shoulder and pelvic girdle muscles. Many of the more than 20 different conditions show overlapping clinical features with other forms of muscular dystrophy, congenital, myofibrillar or even distal myopathies and also with acquired muscle diseases. Although individually extremely rare, all types of LGMD2 together form an important differential diagnostic group among neuromuscular diseases.
The diagnosis includes nothing.
It excludes 2 items.
- Myasthenia gravis or certain specified neuromuscular junction disorders (8C60-8C6Z)
- Secondary myopathies (8C80-8C8Z)
It has no clarifying diagnoses.
The diagnosis is coded elsewhere: