Limb-girdle muscular dystrophy 2B, dysferlin deficiency (Q86047): Difference between revisions
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A distrofia muscular de cinturas autossômica recessiva (LGMD) tipo 2B é um tipo de LGMD, um grupo de distúrbios de fraqueza muscular progressiva, geneticamente determinados, em que a musculatura pélvica ou da cintura escapular está predominantemente ou principalmente envolvida e é caracterizada por pequena cintura escapular envolvimento e envolvimento da panturrilha. | |||
| description / en | description / en | ||
Autosomal recessive limb-girdle muscular dystrophy (LGMD) type 2B is a type of LGMD, a group of genetically determined, progressive muscle weakness disorders, in which the pelvic or shoulder girdle musculature is predominantly or primarily involved, and is characterised by little shoulder girdle involvement and calf involvement. | |||
Revision as of 11:24, 15 August 2026
Autosomal recessive limb-girdle muscular dystrophy (LGMD) type 2B is a type of LGMD, a group of genetically determined, progressive muscle weakness disorders, in which the pelvic or shoulder girdle musculature is predominantly or primarily involved, and is characterised by little shoulder girdle involvement and calf involvement.
| Language | Label | Description | Also known as |
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| default for all languages | ID_370913678 |
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| English | Limb-girdle muscular dystrophy 2B, dysferlin deficiency |
Autosomal recessive limb-girdle muscular dystrophy (LGMD) type 2B is a type of LGMD, a group of genetically determined, progressive muscle weakness disorders, in which the pelvic or shoulder girdle musculature is predominantly or primarily involved, and is characterised by little shoulder girdle involvement and calf involvement. |
