Limb-girdle muscular dystrophy 2G, telethonin gene mutation (Q86065): Difference between revisions

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Latest revision as of 11:25, 15 August 2026

Limb girdle muscular dystrophy (LGMD) type 2G belongs to the group of limb girdle muscular dystrophies which are genetically determined, progressive muscle weakness disorders, in which the pelvic or shoulder girdle musculature is predominantly or primarily involved, and is characterised by anterior distal weakness and rimmed vacuoles.

Language	Label	Description	Also known as
default for all languages	ID_736940214
English	Limb-girdle muscular dystrophy 2G, telethonin gene mutation	Limb girdle muscular dystrophy (LGMD) type 2G belongs to the group of limb girdle muscular dystrophies which are genetically determined, progressive muscle weakness disorders, in which the pelvic or shoulder girdle musculature is predominantly or primarily involved, and is characterised by anterior distal weakness and rimmed vacuoles.