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Samenvatting Screenen toets: oedeem- en vaatafwijkingen - Huidtherapie jaar 2 $5.53   Add to cart

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Samenvatting Screenen toets: oedeem- en vaatafwijkingen - Huidtherapie jaar 2

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In dit document worden alle oedeem- en vaatafwijkingen beschreven. Bij elke diagnose worden de naam, kenmerken, verschillende vormen en behandelingen benoemd. Ook is er minimaal 1 plaatje per afwijking.

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  • November 19, 2023
  • 8
  • 2022/2023
  • Summary
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Oedeem en vaatafwijkingen


 Primair lymfoedeem
 Wordt veroorzaakt door een ontwikkel of functiestoornis van het lymfevatstelsel.
 Partiële dysplasieën(aparte grote&vorm), hypo en hyperplasieën (af&toename
cellen), aplasieën (orgaan niet volledig ontwikkeld), ectasieën (verwijderen)
 Kan 1 of 2 zijdig voorkomen
 Vormen:
o Congenitaal lymfoedeem (aangeboren)
o Lymfoedema precox (rond puberteit)
o Lymfoedema tarda (na 35e levensjaar)




 Congenitaal lymfoedeem
 Ziekte van Milroy: zeldzaam: oedeem aan onderste extremiteiten (meestal
bilateraal). Veroorzaakt door genmutatie
 Soms aanwezig:
o Hydrocele (zwelling balzak)
o Omhoog gerichte teennagels, opgezette tenen
o Papillomatosis
o Syndromen:
o Klippel trenaunav (wijnvlekken, spataderen, afwijkende groei botten)
o Turner (meisjes, 1 x-chromosoom, of 1 van de 2 heeft andere vorm)
o Noonan (trage groei, skelet, verdikking hartspier, vernauwde klep).

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