Limb-girdle muscular dystrophy 1H, gene mapped to 3p25.1p23 (Q84662): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
A distrofia muscular de cinturas tipo 1H (LGMD1H) é uma doença autossômica dominante caracterizada pelo início adulto de fraqueza muscular proximal progressiva que afeta os membros superiores e inferiores. Um locus de doença candidato, dentro de uma região de 25 cM no cromossomo 3p25.1-p23, foi identificado. | |||
| description / en | description / en | ||
Limb-girdle muscular dystrophy type 1H (LGMD1H) is an autosomal dominant disorder characterised by adult onset of progressive proximal muscle weakness affecting both the upper and lower limbs. A candidate disease locus, within a 25-cM region on chromosome 3p25.1-p23, has been identified. | |||
Revision as of 10:00, 15 August 2026
Limb-girdle muscular dystrophy type 1H (LGMD1H) is an autosomal dominant disorder characterised by adult onset of progressive proximal muscle weakness affecting both the upper and lower limbs. A candidate disease locus, within a 25-cM region on chromosome 3p25.1-p23, has been identified.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_320673324 |
||
| English | Limb-girdle muscular dystrophy 1H, gene mapped to 3p25.1p23 |
Limb-girdle muscular dystrophy type 1H (LGMD1H) is an autosomal dominant disorder characterised by adult onset of progressive proximal muscle weakness affecting both the upper and lower limbs. A candidate disease locus, within a 25-cM region on chromosome 3p25.1-p23, has been identified. |
