High Diagnosis Rate for Nonimmune Hydrops Fetalis With Prenatal Clinical Genome: Expanded Results From the Hydrops-Yielding Diagnostic Results of Prenatal Sequencing (HYDROPS) Study.
Aug 2026· American Journal of Medical Genetics. Part A· 0 citations· 20 references
Medicine
TL;DR
ES and GS in NIHF significantly reduce the number of unexplained cases and guide clinical management and recurrence risks, and the incremental diagnostic yield of GS over ES in NIHF remains under investigation.
Abstract
Nonimmune hydrops fetalis (NIHF) is characterized by abnormal fluid accumulation in ≥ 2 fetal compartments and may be genetic. The incremental diagnostic yield of prenatal exome sequencing (ES) for NIHF following a negative standard workup was previously explored on 22 cases. We report ES findings in the remaining cohort and investigate the incremental yield of genome sequencing (GS) in cases without a definitive diagnosis from exome. Enrollment criteria and exome methodology for the Hydrops-Yielding Diagnostic Results of Prenatal Sequencing (HYDROPS) study were previously reported. Exomes without a definitive diagnosis were reviewed with updated clinical information and had GS if DNA was available. A genetic counselor returned the clinical reports. Overall, 50 exomes yielded 22 (44%) diagnoses and six possible diagnoses (12%). Nine new cases (9/28, 68%) had a diagnosis involving one of the following genes: RIT1, SOS1, RYR1, FLT4, LMOD2, KMT2D, PUF60, and BLTP1. Two additional cases were diagnosed upon reclassification of uncertain variants. GS of eligible ES cases resulted in an incremental diagnostic yield of 7% (1/14). ES and GS in NIHF significantly reduce the number of unexplained cases and guide clinical management and recurrence risks. Currently, the incremental diagnostic yield of GS over ES in NIHF remains under investigation. TRIAL REGISTRATION: ClinicalTrials.gov identifier: NCT03911531.
Non-immune hydrops fetalis (NIHF) is a phenotypically heterogeneous condition associated with substantial perinatal morbidity and mortality and its underlying etiology often remains unresolved despite comprehensive conventional investigations. We evaluated the etiological spectrum of NIHF and the additional diagnostic...
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OBJECTIVE
To evaluate the incremental diagnostic yield of sequencing in a large, well-phenotyped international cohort of fetuses with prenatally diagnosed agenesis of the corpus callosum (ACC) and to identify associated genes and variants.
METHODS
Retrospective multicenter cohort study of fetuses with a prenatal diag...
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OBJECTIVE
To present the prenatal sonographic features and genomic spectrum of pregnancies with fetuses with a DLL1 single-nucleotide variant (SNV) or a pure 6q27 deletion.
METHODS
This was a retrospective study of 20 cases with a DLL1 SNV or a pure 6q27 deletion diagnosed by prenatal genetic testing. Clinical and la...
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OBJECTIVE
Prenatal exome sequencing (pES) is increasingly to standard care for diagnosing the etiology of fetal structural anomalies (FSA). We evaluated trio pES outcomes in the national multicentre, prospectively recruited Australian Government-funded cohort, including diagnostic yield, frequency of variants of uncert...
C. Rowntree, Gemma Fernihough, Sarah Long et al.· Prenatal Diagnosis· 0 citations
OBJECTIVE
To characterize the overall diagnostic yield of sequential chromosomal microarray (CMA) and exome sequencing (ES) across the phenotypic spectrum of fetal growth restriction (FGR).
METHODS
A retrospective cohort of 320 consecutive FGR pregnancies presenting at ≥ 20 weeks to a tertiary fetal medicine unit (20...
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