Limb-girdle muscular dystrophy 2I, fukutin related protein gene mutation (Q86058): 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 (LGMD) tipo 2I 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 um espectro clínico que varia de distrofia muscular congênita severa a formas leves de distrofia muscular da cintura dos membros. | |||
| description / en | description / en | ||
Limb girdle muscular dystrophy (LGMD) type 2I 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 a clinical spectrum ranging from severe congenital muscular dystrophy to mild forms of limb girdle muscular dystrophy. | |||
Revision as of 11:25, 15 August 2026
Limb girdle muscular dystrophy (LGMD) type 2I 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 a clinical spectrum ranging from severe congenital muscular dystrophy to mild forms of limb girdle muscular dystrophy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1951243194 |
||
| English | Limb-girdle muscular dystrophy 2I, fukutin related protein gene mutation |
Limb girdle muscular dystrophy (LGMD) type 2I 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 a clinical spectrum ranging from severe congenital muscular dystrophy to mild forms of limb girdle muscular dystrophy. |
