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Resolving Severe Oligohydramnios as an Early Prenatal Presentation of Renal Coloboma Syndrome - a Report of Two Generations
  • +1
  • Andrew Nguyen,
  • Carla Campagnolo,
  • Ghislain Hardy,
  • Maha Saleh
Andrew Nguyen
Schulich School of Medicine and Dentistry
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Carla Campagnolo
London Health Sciences Centre
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Ghislain Hardy
Schulich School of Medicine and Dentistry
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Maha Saleh
Schulich School of Medicine and Dentistry
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Abstract

Renal coloboma syndrome (RCS) is an autosomal dominant disorder associated with the PAX2 gene. With variable expressivity, renal and ocular abnormalities are reported in a majority of individuals affected. We highlight a mother and her newborn with RCS, both presenting prenatally, showing self-resolving severe oligohydramnios as an early prenatal finding.

Peer review status:ACCEPTED

07 Jun 2021Submitted to Clinical Case Reports
11 Jun 2021Submission Checks Completed
11 Jun 2021Assigned to Editor
19 Jun 2021Reviewer(s) Assigned
25 Jun 2021Review(s) Completed, Editorial Evaluation Pending
28 Jun 2021Editorial Decision: Revise Minor
22 Jul 20211st Revision Received
23 Jul 2021Submission Checks Completed
23 Jul 2021Assigned to Editor
23 Jul 2021Review(s) Completed, Editorial Evaluation Pending
23 Jul 2021Editorial Decision: Accept