Autosomal recessive muscular dystrophy, childhood type, resembling Becker muscular dystrophy (Q93408): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| Property / Collection date | |||||||||||||||
15 August 2026
| |||||||||||||||
| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 08:30, 16 August 2026
Childhood autosomal recessive muscular dystrophy resembling Becker disease is a rare condition characterised by muscular dystrophy with mild, Becker-like progression, affecting both sexes equally. It refers to a genetically heterogeneous group of disorders in which different molecular and biochemical defects present with a similar phenotype. Most patients have defects in one of the four sarcoglycan genes identified to date.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_391677057 |
||
| English | Autosomal recessive muscular dystrophy, childhood type, resembling Becker muscular dystrophy |
Childhood autosomal recessive muscular dystrophy resembling Becker disease is a rare condition characterised by muscular dystrophy with mild, Becker-like progression, affecting both sexes equally. It refers to a genetically heterogeneous group of disorders in which different molecular and biochemical defects present with a similar phenotype. Most patients have defects in one of the four sarcoglycan genes identified to date. |
Statements
CID11:ID_391677057
0 references
dki-india-ID_391677057
0 references
Concluído
0 references
15 August 2026
0 references
