Congenital myotonic dystrophy (Q101370): Difference between revisions
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A distrofia miotônica congênita (DMC) é um distúrbio muscular caracterizado por hipotonia severa e fraqueza ao nascimento, frequentemente com insuficiência respiratória. A forma grave demonstra um curso “bifásico” único, por isso os sintomas neonatais melhoram ou se estabilizam em neonatos sobreviventes, antes que os sintomas do tipo adulto se apresentem posteriormente. | |||
| description / en | description / en | ||
Congenital myotonic dystrophy (CDM) is a muscle disorder characterised by severe hypotonia and weakness at birth, often with respiratory insufficiency. Severe form demonstrates a unique “biphasic” course, hereby neonatal symptoms improve or stabilise in surviving neonates, before adult-type symptoms present in later life. | |||
Revision as of 18:10, 16 August 2026
Congenital myotonic dystrophy (CDM) is a muscle disorder characterised by severe hypotonia and weakness at birth, often with respiratory insufficiency. Severe form demonstrates a unique “biphasic” course, hereby neonatal symptoms improve or stabilise in surviving neonates, before adult-type symptoms present in later life.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_599230687 |
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| English | Congenital myotonic dystrophy |
Congenital myotonic dystrophy (CDM) is a muscle disorder characterised by severe hypotonia and weakness at birth, often with respiratory insufficiency. Severe form demonstrates a unique “biphasic” course, hereby neonatal symptoms improve or stabilise in surviving neonates, before adult-type symptoms present in later life. |
