Duchenne muscular dystrophy (Q41380): 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 | ||
Distrofia muscular de Duchenne (DMD) é uma miopatia grave ligada ao X causada por mutação no gene da distrofina, com sintomas aparecendo antes dos 6 anos de idade com uma rápida progressão da doença. Sintomas podem incluir fadiga, dificuldades de aprendizagem (o QI pode estar abaixo de 75), fraqueza muscular, problemas com habilidades motoras, quedas frequentes e dificuldade progressiva para andar. | |||
| description / en | description / en | ||
Duchenne muscular dystrophy (DMD) is a severe X-linked myopathy caused by mutation in the dystrophin gene with symptoms appearing before the age of 6 with a rapid disease progression. Symptoms may include fatigue, learning difficulties (the IQ can be below 75), Muscle weakness, problems with motor skills, frequent falls and progressive difficulty walking. | |||
Revision as of 07:31, 13 August 2026
Duchenne muscular dystrophy (DMD) is a severe X-linked myopathy caused by mutation in the dystrophin gene with symptoms appearing before the age of 6 with a rapid disease progression. Symptoms may include fatigue, learning difficulties (the IQ can be below 75), Muscle weakness, problems with motor skills, frequent falls and progressive difficulty walking.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 8C70.1 |
||
| English | Duchenne muscular dystrophy |
Duchenne muscular dystrophy (DMD) is a severe X-linked myopathy caused by mutation in the dystrophin gene with symptoms appearing before the age of 6 with a rapid disease progression. Symptoms may include fatigue, learning difficulties (the IQ can be below 75), Muscle weakness, problems with motor skills, frequent falls and progressive difficulty walking. |
