Resolving Severe Oligohydramnios as an Early Prenatal Presentation of
Renal Coloboma Syndrome - a Report of Two Generations
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.