Prenatal phenotype of Kabuki syndrome: A case series and literature review
Prenatal Diagnosis2021Vol. 41(9), pp. 1089–1100
Citations Over TimeTop 14% of 2021 papers
Po Lam So, Ho‐Ming Luk, Ka Wang Cheung, Winnie W. I. Hui, Man Yan Chung, A. Mak, Wing Yi Lok, Kris P. T. Yu, Shirley S. W. Cheng, Edgar W. L. Hau, Stephanie Ho, Stephen T.S. Lam, Ivan F. M. Lo
Abstract
These cases demonstrate the prenatal phenotypic heterogeneity associated with KS. Although the ultrasound abnormalities are non-specific, KS should be considered in the differential diagnosis when these fetal findings following normal microarray analysis/karyotyping.
Related Papers
- → The natural history of oligohydramnios/polyhydramnios sequence in monochorionic diamniotic twins(1992)35 cited
- → Acute reversal of oligohydramnios‐polyhydramnios sequence in monochorionic twins(1996)9 cited
- → Polyhydramnios and Oligohydramnios(2007)9 cited
- → Polyhydramnios and Oligohydramnios(2012)1 cited
- → Can hematologic parameters predict isolated oligohydramnios and isolated polyhydramnios?(2023)