Spheroid body myopathy (Q90771): 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 miopatia com corpos esferóides é uma doença rara classificada no grupo das miopatias congênitas como um distúrbio neuromuscular relacionado à desmina, apresentando origem autossômica dominante com início dos sintomas na fase adulta. A biópsia muscular revela corpos citoplasmáticos esferóides característicos. | |||
| description / en | description / en | ||
Spheroid body myopathy is a rare illness classified in the group of the congenital myopathies as a desmin-related neuromuscular disorder, presenting dominant autosomical origin with the beginning of the symptoms in the adult phase. Muscle biopsy discloses characteristic spheroid cytoplasmic bodies. | |||
Revision as of 17:45, 15 August 2026
Spheroid body myopathy is a rare illness classified in the group of the congenital myopathies as a desmin-related neuromuscular disorder, presenting dominant autosomical origin with the beginning of the symptoms in the adult phase. Muscle biopsy discloses characteristic spheroid cytoplasmic bodies.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_83824621 |
||
| English | Spheroid body myopathy |
Spheroid body myopathy is a rare illness classified in the group of the congenital myopathies as a desmin-related neuromuscular disorder, presenting dominant autosomical origin with the beginning of the symptoms in the adult phase. Muscle biopsy discloses characteristic spheroid cytoplasmic bodies. |
