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 / endescription / 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.
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Property / Canonical URI: https://id.who.int/icd/entity/599230687 / rank
 
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CID11:ID_599230687
Property / CURIE: CID11:ID_599230687 / rank
 
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dki-india-ID_599230687
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Concluído
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Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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15 August 2026
Timestamp+2026-08-15T00:00:00Z
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CalendarGregorian
Precision1 day
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Property / Collection date: 15 August 2026 / rank
 
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Latest 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.
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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.

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      CID11:ID_599230687
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      dki-india-ID_599230687
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      Concluído
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      15 August 2026
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