Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Hereditary Anemias as a Monogenic Etiology for Nonimmune Hydrops Fetalis.

Clinical therapeutics - 1 Jul 2026

Makhamreh Mona M, Rice Stephanie M, Shivashankar Kavya, Brewer Casey J, McLaren Rodney A, Berger Seth I, Al-Kouatly Huda B

Abstract excerpt

PURPOSE: Hereditary anemias are a cause of nonimmune hydrops fetalis (NIHF). Our objective was to review the spectrum of hereditary anemia genes in NIHF diagnosed by exome sequencing (ES). METHODS: We performed a systematic review of ES studies in NIHF from January 1, 2000 to August 1, 2024 with emphasis on genes causing fetal anemia as a primary phenotype. FINDINGS: Forty-one ES studies with 207 genetically...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Anemia
Share to Exome Sequencing
Share to Hydrops Fetalis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Phenotype

Share to Pregnancy

Source

Identifiers

PMID: 41638966
DOI: 10.1016/j.clinthera.2026.01.002

Genes

KLF1
RPL11
SEC23B
SPTA1
UNC13D

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hereditary Anemias as a Monogenic Etiology for Nonimmune Hydrops Fetalis.PMID 41638966Read ↗

RASopathies are the most common set of monogenic syndromes identified by exome sequencing for nonimmune hydrops fetalis: A systematic review and meta-analysis.Semantic proximity Read ↗

The many etiologies of nonimmune hydrops fetalis diagnosed by exome sequencingSemantic proximity Read ↗

Diagnostic yield using whole‐genome sequencing and in‐silico panel of 281 genes associated with non‐immune hydrops fetalis in clinical settingSemantic proximity Read ↗

Utility of fetal whole exome sequencing in the etiological evaluation and outcome of nonimmune hydrops fetalisSemantic proximity Read ↗

Nonimmune hydrops fetalis: Genetic analysis and clinical outcomeSemantic proximity Read ↗

Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis.Semantic proximity Read ↗

Value of Exome Sequencing in Diagnosis and Management of Recurrent Non-immune Hydrops Fetalis: A Retrospective AnalysisSemantic proximity Read ↗

PIEZO1 is the most common monogenic etiology of non‐immune hydrops fetalis detected by prenatal exome sequencingSemantic proximity Read ↗

Fetal hydrops and the Incremental yield of Next‐generation sequencing over standard prenatal Diagnostic testing ( FIND ) study: prospective cohort study and meta‐analysisSemantic proximity Read ↗

Non-immune hydrops fetalis is associated with bi-allelic pathogenic variants in the MYB Binding Protein 1a (MYBBP1A) gene.Semantic proximity Read ↗

Lysosomal storage disorders in nonimmune hydrops fetalis diagnosed by exome sequencingSemantic proximity Read ↗

Resolving fetal hydrops - A rare entity.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.