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Myotone Dystrofie Type 1.pdf

Brochure-Neurologische-zorg-myotone-dystrofie-type-1.pdf
Preview of Myotone Dystrofie Type 1
🔗 Source: mdexpertisecentrum.nl
📊 Size: 368 KB
📄 Pages: 15 pages
⬇️ Downloads: 124

Summary

Myotone dystrofie type 1 (MD 1) kenmerkt zich door toenemende spierzwakte en myotonie, en kan ook andere organen, waaronder de hersenen, aantasten. Mensen met MD 1 zijn zich vaak niet bewust van veranderingen in hun gedrag of gevoelsleven, maar deze veranderingen kunnen een grote last zijn voor de omgeving. De ziekte heeft vier vormen: congenitale, kinder-, volwassen- en milde vorm, elk met eigen symptomen en beginleeftijd. Behandeling omvat medicatie voor myotonie, behandeling van nachtelijke hypoventilatie, cognitieve gedragstherapie voor vermoeidheid en verwijzing naar een revalidatiearts of psycholoog. Een individueel zorgplan is essentieel voor adequate zorg.

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Description

Myotone dystrofie type 1 (MD 1) kenmerkt zich door toenemende spierzwakte en myotonie, en kan ook andere organen, waaronder de hersenen, aantasten.

Technical Information

  • File Format: PDF
  • File Size: 368 KB
  • Pages: 15
  • Language: NL
  • Total Downloads: 124
  • Last Updated: 1 week ago

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This PDF document about Myotone Dystrofie Type 1 provides comprehensive information and guidance. Whether you're a beginner or advanced user, this resource offers valuable insights into Myotone Dystrofie Type 1.

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