Resolving severe oligohydramnios as an early prenatal presentation of renal coloboma syndrome—A report of two generations-Reference-Cited by-同舟云学术

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Resolving severe oligohydramnios as an early prenatal presentation of renal coloboma syndrome—A report of two generations

Published:2021-09 Issue:9 Volume:9 Page:
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clin Case Rep

Author:

Nguyen Andrew¹^ORCID,Campagnolo Carla²,Hardy Ghislain¹³,Saleh Maha¹²^ORCID

Affiliation:

1. Schulich School of Medicine and Dentistry University of Western Ontario London ON Canada

2. Department of Paediatrics Division of Genetics and Metabolism London Health Sciences Centre London ON Canada

3. Department of Obstetrics and Gynecology London Health Sciences Centre London ON Canada

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.4758

Reference10 articles.

1. BowerMA SchimmentiLA EcclesMR.PAX2‐related disorder.https://www.ncbi.nlm.nih.gov/books/NBK1451/. Accessed January 4 2021.

2. Renal coloboma syndrome

3. Renal-coloboma syndrome: Prenatal detection and clinical spectrum in a large family

4. Analysis of prenatal phenotype and pathogenetic variant in a fetus with Papillorenal syndrome;Li J;Chinese J Med Genet,2020

5. PAX2mutations in fetal renal hypodysplasia

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