Prenatal Diagnosis of 5p Deletion Syndrome with Brain Abnormalities by Ultrasonography and Fetal Magnetic Resonance Imaging: A Case Report-Reference-Cited by-同舟云学术

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Prenatal Diagnosis of 5p Deletion Syndrome with Brain Abnormalities by Ultrasonography and Fetal Magnetic Resonance Imaging: A Case Report

Published:2019-09-25 Issue:5 Volume:39 Page:446-451
ISSN:1551-3815
Container-title:Fetal and Pediatric Pathology
language:en
Short-container-title:Fetal and Pediatric Pathology

Author:

Kaymak Didem¹,Alpay Verda¹,Erenel Hakan²^ORCID,Adaletli İbrahim³,Comunoglu Nil⁴,Madazli Riza¹

Affiliation:

1. Department of Obstetrics and Gynecology, Faculty of Medicine, Istanbul University Cerrahpasa, Istanbul, Turkey;

2. Department of Obstetrics and Gynecology, Division of Perinatology, Faculty of Medicine, Istanbul University Cerrahpasa, Istanbul, Turkey;

3. Department of Radiology, Faculty of Medicine, Istanbul University Cerrahpasa, Istanbul, Turkey;

4. Department of Pathology, Faculty of Medicine, Istanbul University Cerrahpasa, Istanbul, Turkey

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/15513815.2019.1669230

Reference18 articles.

1. 5p deletions: Current knowledge and future directions

2. The cri du chat syndrome

3. Ultrasonography of the fetal brainstem: a biometric and anatomical, multioperator, cross-sectional study of 913 fetuses of 21-36 weeks of gestation

4. Nomograms of the axial fetal cerebellar hemisphere circumference and area throughout gestation

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Prenatal Sonographic Features of Cri-du-Chat Syndrome: A Case Report and Analytical Literature Review;Diagnostics;2022-02-06

2. Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations;European Journal of Paediatric Neurology;2020-09

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