Abstract

Şizensefali, pial membrandan lateral ventrikül ependimal yüzeyine uzanan yarıklarla karakterize bir nöronal migrasyon anomalisidir. Hastalar genellikle mental retardasyon, hemiparezi, gelişimsel defisitler ve epileptik nöbetlerle prezente olmaktadır. Şizensefalinin en yaygın sebepleri prenatal infeksiyonlar, maternal travma, hipoksemi ve EMX2 mutasyonlarıdır. Şizensefali tanısında tercih edilen yöntem manyetik rezonans görüntülemedir. Bu olgu sunumunda şizensefali saptanan 11 aylık erkek bebek sunulacaktır.

Alternate abstract:

Schizencephaly, a neuronal migration abnormality, is characterized with clefts that extend from the pial membrane to the ependymal surface of the lateral ventricle. Patients usually present with mental retardation, hemiparesis, developmental deficits and epileptic seizures. The most common causes of schizencephaly are prenatal infections, maternal trauma, hypoxemia and EMX2 mutations. The method of choice in diagnosis of schizencephaly is magnetic resonance imaging. In this case report, an 11-month-old male infant with schizencephaly will be presented.

Details

Title
Şizensefali
Author
ŞİRİN, Büşra  VIAFID ORCID Logo  ; KESİKTAŞ, Nur  VIAFID ORCID Logo  ; ERSOY, Sedef  VIAFID ORCID Logo 
Pages
201-204
Section
Olgu Sunumu
Publication year
2022
Publication date
2022
Publisher
Pamukkale University, Facutly of Medicine
ISSN
13099833
e-ISSN
13080865
Source type
Scholarly Journal
Language of publication
Turkish
ProQuest document ID
2694008703
Copyright
© 2022. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.