Limb-girdle muscular dystrophy 2G, telethonin gene mutation (Q86065): Difference between revisions
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A distrofia muscular de cinturas (LGMD) tipo 2G pertence ao grupo de distrofias musculares da cintura escapular que são geneticamente determinadas, distúrbios de fraqueza muscular progressiva, em que a musculatura pélvica ou da cintura escapular está predominantemente ou principalmente envolvida, e é caracterizada por fraqueza distal anterior e vacúolos marginados. | |||
| description / en | description / en | ||
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. | |||
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 |
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| 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. |
