Congenital myotonic dystrophy (Q101370): Difference between revisions
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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. |
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CID11:ID_599230687
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dki-india-ID_599230687
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