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Article

Prenatal phenotype of 10p15.3 microdeletion syndrome: A series of five cases.

Taiwanese journal of obstetrics & gynecology - 1 Jul 2026

Jing Xiang-Yi, Zhen Li, Li Dong-Zhi

Abstract excerpt

OBJECTIVE: The aim of the study was to present the fetal features of chromosome 10p15.3 microdeletion syndrome to gain awareness that the antenatal characteristics can be very nonspecific. CASE REPORT: This was a retrospective study of five cases with 10p15.3 microdeletion syndrome diagnosed in utero. Two cases were diagnosed in the first trimester because of increased nuchal translucency (NT). Three had normal...

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Share to Chromosome Deletion
Share to Chromosomes, Human, Pair 10
Share to Fetal Growth Retardation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Ultrasonography, Prenatal

Source

Identifiers

PMID: 42362275
DOI: 10.1016/j.tjog.2024.01.040

Genes

FGR
ZMYND11

Provenance

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

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