Certain specified rare distal myopathy (Q85565): 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 | ||
Doenças genéticas progressivas raras caracterizadas por atrofia e fraqueza dos músculos voluntários das extremidades distais dos membros superiores e inferiores. Embora a idade de início possa ocorrer a qualquer momento, desde a infância até a idade adulta, a maioria das formas se desenvolve mais tarde na vida e é lentamente progressiva. A herança é autossômica dominante ou recessiva. | |||
| description / en | description / en | ||
Rare progressive genetic disorders characterised by wasting and weakness of the voluntary muscles of the distal extremities of upper and lower limbs. Although age of onset can occur anytime from infancy to adulthood, most forms develop later in life and are slowly progressive. Inheritance is autosomal dominant or recessive. | |||
Revision as of 10:55, 15 August 2026
Rare progressive genetic disorders characterised by wasting and weakness of the voluntary muscles of the distal extremities of upper and lower limbs. Although age of onset can occur anytime from infancy to adulthood, most forms develop later in life and are slowly progressive. Inheritance is autosomal dominant or recessive.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1760014100 |
||
| English | Certain specified rare distal myopathy |
Rare progressive genetic disorders characterised by wasting and weakness of the voluntary muscles of the distal extremities of upper and lower limbs. Although age of onset can occur anytime from infancy to adulthood, most forms develop later in life and are slowly progressive. Inheritance is autosomal dominant or recessive. |
