Schizencephaly accompanied by occipital encephalocele and deletion of chromosome 22q13.32: a case report-Reference-Cited by-同舟云学术

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Schizencephaly accompanied by occipital encephalocele and deletion of chromosome 22q13.32: a case report

Published:2019-05-26 Issue:6 Volume:38 Page:496-502
ISSN:1551-3815
Container-title:Fetal and Pediatric Pathology
language:en
Short-container-title:Fetal and Pediatric Pathology

Author:

Inan Cihan¹,Sayin N. Cenk¹,Gurkan Hakan²,Atli Engin²,Gursoy Erzincan Selen¹,Uzun Isil¹,Sutcu Havva¹,Dogan Sumeyra³,Ikbal Atli Emine²,Varol Fusun¹

Affiliation:

1. Division of Perinatology, Department of Obstetrics & Gynecology, Faculty of Medicine, Trakya University, Edirne, Turkey;

2. Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey;

3. Department of Radiology, Faculty of Medicine, Trakya University, Edirne, Turkey

Publisher

Informa UK Limited

Subject

General Medicine,Pathology and Forensic Medicine,Pediatrics, Perinatology, and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/15513815.2019.1604921

Reference21 articles.

1. Schizencephaly prevalence, prenatal diagnosis and clues to etiology: a register-based study

2. Prenatal Diagnosis and Postnatal Outcome of Schizencephaly

3. Schizencephaly of open and closed lip type in the same patient: An extremely rare occurrence

4. Schizencephaly—diagnostics and clinical dilemmas

5. Schizencephaly: correlation between the lobar topography of the cleft(s) and absence of the septum pellucidum

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