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Lissencefalie als gevolg van LIS1-mutatie
Lissencefalie door LIS1-mutatie

Vertaling van "lissencefalie door lis1-mutatie " (Nederlands → Engels) :

lissencefalie door LIS1-mutatie

A cerebral malformation with epilepsy with predominant characteristics of posterior isolated lissencephaly with developmental delay, intellectual disability and epilepsy that usually evolves from West syndrome to Lennox-Gastaut syndrome. Additional f


lissencefalie als gevolg van LIS1-mutatie

A cerebral malformation with epilepsy with predominant characteristics of posterior isolated lissencephaly with developmental delay, intellectual disability and epilepsy that usually evolves from West syndrome to Lennox-Gastaut syndrome. Additional f


lissencefalie type 1 door mutatie van 'doublecortin'-gen

A semi-dominant X-linked disease with intellectual deficiency and seizures that is more severe in male patients. Boys presenting with lissencephaly show an abnormally thick cortex with very few gyri (pachygyria) or even none (agyria). Clinical manife




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Date index: 2021-02-21
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