Titin-related limb-girdle muscular dystrophy R10

Orpha code: 140922OMIM code: 608807

Definicja

A form of limb-girdle muscular dystrophy that usually has a childhood onset (but can range from the first to third decade of life) of severe progressive proximal weakness, eventually involving the distal muscles. Some patients may remain ambulatory but most are wheelchair dependant 20 years after onset.

Disease data
Klasyfikacja

Disease

Synonimy
Autosomal recessive limb-girdle muscular dystrophy type 2J
LGMD2J
LGMD type 2J
LGMD2J
Limb-girdle muscular dystrophy type 2J
Titin-related LGMD R10
Kod ORPHA
140922
Kod OMIM
608807
Kod ICD10
G71.0
Kod ICD11
-

No additional description.

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