APOE epsilon 4: a potential modulation factor in Rett syndrome

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F10%3A7030" target="_blank" >RIV/00216208:11110/10:7030 - isvavai.cz</a>
Alternative codes found
RIV/00064165:_____/10:7030
Result on the web
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DOI - Digital Object Identifier
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Result language
angličtina
Original language name
APOE epsilon 4: a potential modulation factor in Rett syndrome
Original language description
Rett syndrome is a neurodevelopmental disorder mainly caused by de novo mutations in the MECP2 (methyl-CpG-binding protein 2) gene. There is considerable variation in the severity of clinical features among Rett syndrome patients, even among patients with the same MECP2 mutation. In addition to X-chromosome inactivation pattern, the genetic background of the affected individual might also have a role in determining the severity of the disorder. We suggest that APOE is one of the genetic modulating factors. We analyzed clinical phenotypes of 46 patients with Rett syndrome, with confirmed MECP2 mutation. We discovered that among epsilon 4 carriers, some clinical features were more severe, and the developmental regression occurred 4 months earlier on average than in those without the e4 allele.
Czech name
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Czech description
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Project
<a href="/en/project/NR9215" target="_blank" >NR9215: Molecular pathology and pathophysiology of neurodegenerative diseases accompanied by movement disorders</a>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP) Z - Vyzkumny zamer (s odkazem do CEZ) S - Specificky vyzkum na vysokych skolach

Publication year
2010
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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