Cargando…
Resolving severe oligohydramnios as an early prenatal presentation of renal coloboma syndrome—A report of two generations
This report suggests that self‐resolving oligohydramnios is an early sign of malfunctioning kidney in individuals with renal coloboma syndrome (RCS) and demonstrates how a genetic diagnosis can impact patient and fetal management as it outlines two generations of RCS.
Autores principales: | Nguyen, Andrew, Campagnolo, Carla, Hardy, Ghislain, Saleh, Maha |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8423080/ https://www.ncbi.nlm.nih.gov/pubmed/34512982 http://dx.doi.org/10.1002/ccr3.4758 |
Ejemplares similares
-
TP63‐mutation as a cause of prenatal lethal multicystic dysplastic kidneys
por: Friedmann, Isabel, et al.
Publicado: (2020) -
Renal coloboma syndrome with epilepsy
por: Li, Jitong, et al.
Publicado: (2021) -
Alagille syndrome due to a de novo NOTCH2 mutation presenting as prenatal oligohydramnios and congenital bilateral renal hypodysplasia: A case report
por: Xu, Fengdan, et al.
Publicado: (2022) -
Heparin successfully improved an early onset intrauterine growth restriction accompanied by severe oligohydramnios
por: Chu, Hong-Nü
Publicado: (2009) -
A Premature Baby with Severe Oligohydramnios and Hypotension: a Case Report of Renal Tubular Dysgenesis
por: Min, Jeesu, et al.
Publicado: (2020)