Prenatally diagnosed distal 16p11.2 microdeletion with a novel association with congenital diaphragmatic hernia: a case report-Reference-Cited by-同舟云学术

Prenatally diagnosed distal 16p11.2 microdeletion with a novel association with congenital diaphragmatic hernia: a case report

Published:2018-02-09 Issue:4 Volume:6 Page:592-595
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clin Case Rep

Author:

Genesio Rita¹,Maruotti Giuseppe Maria²,Saccone Gabriele²,Mormile Angela¹,Conti Anna¹^ORCID,Cicatiello Rita¹,Sarnataro Viviana¹,Sirico Angelo²^ORCID,Izzo Antonella¹,Martinelli Pasquale²,Nitsch Lucio¹

Affiliation:

1. Department of Molecular Medicine and Medical Biotechnology; School of Medicine; University of Naples Federico II; Naples Italy

2. Department of Neuroscience, Reproductive Sciences and Dentistry; School of Medicine; University of Naples Federico II; Naples Italy

Funder

Regione Campania

Publisher

Wiley

Subject

General Medicine

Reference16 articles.

1. An evidence-based review of the current treatment of congenital diaphragmatic hernia;Haroon;Clin. Pediatr.,2013

2. Outcomes of congenital diaphragmatic hernia in the modern era of management;Wynn;J. Pediatr.,2013

3. Associated malformations in congenital diaphragmatic hernia;Zaiss;Am. J. Perinatol.,2011

4. De novo copy number variants are associated with congenital diaphragmatic hernia;Yu;J. Med. Genet.,2012

5. Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic hernia;Wat;J. Med. Genet.,2011

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1. Prenatal phenotypes and pregnancy outcomes of fetuses with 16p11.2 microdeletion/microduplication;BMC Pregnancy and Childbirth;2024-07-22

2. Health supervision for children and adolescents with 16p11.2 deletion syndrome;Molecular Case Studies;2023-12

3. Clinical outcomes of fetuses with chromosome 16 short arm copy number variants;Molecular Genetics & Genomic Medicine;2023-04-04

4. Molecular cytogenetic characterization of 16p11.2 microdeletions with diverse prenatal phenotypes: Four cases report and literature review;Taiwanese Journal of Obstetrics and Gynecology;2022-05

5. Fetal intracranial hemorrhage in a case of 16p microdeletion;Case Reports in Perinatal Medicine;2022-01-01