Evidence map›Paper›PMID 39218907›Full record

ArticleMolecular cytogenetics2024

Prenatal diagnosis of fetuses with 15q11.2 BP1-BP2 microdeletion in the Chinese population: a seven-year single-center retrospective study.

Jianlong Zhuang, Na Zhang, Wanyu Fu, Yuying Jiang, Yu'e Chen, Chunnuan Chen

Abstract read
In one paragraph

Article in Molecular cytogenetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Jianlong Zhuang *Prenatal diagnosis center, Quanzhou Women's and Children's Hospital, Quanzhou, 362000, Fujian Province, China. 415913261@qq.com.
Na Zhang *Prenatal diagnosis center, Quanzhou Women's and Children's Hospital, Quanzhou, 362000, Fujian Province, China.
Wanyu FuPrenatal diagnosis center, Quanzhou Women's and Children's Hospital, Quanzhou, 362000, Fujian Province, China.
Yuying JiangPrenatal diagnosis center, Quanzhou Women's and Children's Hospital, Quanzhou, 362000, Fujian Province, China.
Yu'e ChenDepartment of Ultrasound, Quanzhou Women's and Children's Hospital, Quanzhou, 362000, Fujian Province, China. 26608708@qq.com.
Chunnuan ChenDepartment of Neurology, Second Affiliated Hospital of Fujian Medical University, Quanzhou, 362000, Fujian Province, China. chenchunnuan1983@aliyun.com.

Funding

Quanzhou City Science and Technology Program 2023NS068
6 · The paper itself

Abstract

backgroundThe 15q11.2 BP1-BP2 microdeletion syndrome is associated with developmental delays, language impairments, neurobehavioral disorders, and psychiatric complications. The aim of the present study was to provide prenatal and postnatal clinical data for 16 additional fetuses diagnosed with the 15q11.2 BP1-BP2 microdeletion syndrome in the Chinese population.

methodsA total of 5,789 pregnancy women that underwent amniocentesis were enrolled in the present study. Both karyotype analysis and chromosomal microarray analysis (CMA) were conducted on these subjects to detect chromosomal abnormalities and copy number variants (CNVs). Whole exome sequencing (WES) was performed to investigate sequence variants in subjects with clinical abnormalities after birth.

resultsSixteen fetuses with 15q11.2 BP1-BP2 microdeletion were identified in the present study, with a detection rate of 0.28% (16/5,789). The 15q11.2 BP1-BP2 microdeletion fragments ranged from 311.8 kb to 849.7 kb, encompassing the NIPA1, NIPA2, CYFIP1, and TUBGCP5 genes. The follow-up results regarding pregnancy outcomes showed that five cases opted for pregnancy termination, while the remaining cases continued with their pregnancies. Subsequent postnatal follow-up indicated that only one case with the 15q11.2 BP1-BP2 microdeletion displayed neurodevelopmental disorders, demonstrating an incomplete penetrance rate of 9.09% (1/11).

conclusionThe majority of fetuses with the 15q11.2 microdeletion exhibit typical features during early childhood, indicating a low penetrance and mild impact. Nonetheless, pregnancies involving fetuses with the 15q11.2 microdeletion require thorough prenatal counseling. Additionally, enhanced supervision and extended postnatal monitoring are warranted for those who choose to proceed with their pregnancies.

Indexed as

15q11.2 BP1-BP2 microdeletionChromosomal microarray analysisKaryotype analysisPrenatal diagnosisWhole exome sequencing

Identifiers

PMID39218907
PMCPMC11367773

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.