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Article

Prenatal diagnosis of 15q13.3 deletion and duplication syndrome: what do we tell the prospective parents?

Archives of gynecology and obstetrics - 1 Dec 2025

Luo Xiaojin, Liu Hongqing, Chen Xiaohang, Niu Hongyan, Zhou Fei, Zeng Shuxian, Fu Yuhe, Liu Jinxing, Guo Yanyun

Abstract excerpt

OBJECTIVE: This retrospective study analyzed ultrasound findings, single nucleotide polymorphism microarray (SNP array) results, pregnancy outcomes, and postnatal follow-up data in fetuses with 15q13.3 deletions or duplications. METHODS: Six fetuses were diagnosed with 15q13.3 deletions and nine with 15q13.3 duplications via SNP array at the prenatal diagnosis center of a single tertiary medical center from...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 41123664
DOI: 10.1007/s00404-025-08150-z
PMCID: PMC12705849

Genes

CHRNA7
KLF13
MTMR10
OTUD7A
TRPM1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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