Congenital myotonic dystrophy (Q101370): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed label, description and/or aliases in pt-br, en |
Changed an Item |
||
| Property / Canonical URI | |||
| Property / Canonical URI: https://id.who.int/icd/entity/599230687 / rank | |||
Normal rank | |||
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 |
||
| 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. |
