{
  "abstract": "Objective\n\nTo evaluate the diagnostic yield and clinical value of a phenotype-driven genomic testing strategy in fetuses with central nervous system (CNS) abnormalities.Methods\n\nIn this retrospective single-center study, 966 fetuses with CNS abnormalities detected by prenatal ultrasound and/or fetal magnetic resonance imaging were included. All cases underwent copy number variation sequencing (CNV-seq), while karyotyping and trio exome sequencing (trio-ES) were performed based on clinical indications and parental preference. Fetuses were stratified into isolated-single, isolated-complex, and non-isolated subgroups according to CNS involvement and extracranial abnormalities. Diagnostic yields were compared across phenotypic subgroups and common CNS phenotypes.Results\n\nAmong 966 fetuses with prenatal CNS abnormalities, pathogenic or likely pathogenic (P/LP) variants were identified in 12.63% of cases. CNV-seq had a diagnostic yield of 8.07% (78/966), while trio-ES had a diagnostic yield of 16.32% (70/429) and provided an additional 10.92% yield (44/403) following negative CNV-seq results. Diagnostic yield varied significantly across phenotypic subgroups, with a higher CNV-seq yield in non-isolated cases than in isolated cases (15.41% vs. 4.25%, P < 0.001), and a higher ES yield in isolated-complex cases than in isolated-single cases (32.56% vs. 9.20%, P < 0.001). After excluding mild isolated CNS anomalies, diagnostic yields increased to 15.60% for CNV-seq and 26.67% for ES. In the adjusted cohort, differences among the three subgroups remained significant for CNV-seq (P < 0.001) but not for ES (P = 0.156). Across phenotypes, major structural abnormalities demonstrated substantially higher diagnostic yields than mild or soft markers, with a clear severity-dependent increase observed in ventriculomegaly and head circumference reduction.Conclusion\n\nFetal CNS abnormalities show substantial genetic heterogeneity, and diagnostic yield is closely associated with prenatal imaging phenotypes. A phenotype-driven testing strategy may help prioritize genetic evaluation and improve prenatal counseling for fetuses with CNS abnormalities.",
  "abstract_shown": true,
  "affiliations": [
    "Department of Medical Genetics, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing Maternal and Child Health Care Hospital, Beijing, 100026, China.",
    "Prenatal Diagnosis Center, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing Maternal and Child Health Care Hospital, Beijing, 100026, China.",
    "Department of Medical Genetics, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing Maternal and Child Health Care Hospital, Beijing, 100026, China. yys_521@ccmu.edu.cn.",
    "Department of Central Laboratory, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing Maternal and Child Health Care Hospital, Beijing, 100010, China. yinchh@ccmu.edu.cn."
  ],
  "article_type": "research article",
  "arxiv": null,
  "author_total": 10,
  "authors": [
    {
      "affs": [
        0
      ],
      "name": "Xinyu Fu"
    },
    {
      "affs": [
        0
      ],
      "name": "Wei Zhong"
    },
    {
      "affs": [
        0
      ],
      "name": "Zhengyang Yao"
    },
    {
      "affs": [
        0
      ],
      "name": "Huimin Gao"
    },
    {
      "affs": [
        0
      ],
      "name": "Fang Wang"
    },
    {
      "affs": [
        1
      ],
      "name": "Yan Liu"
    },
    {
      "affs": [
        1
      ],
      "name": "Yifan Liu"
    },
    {
      "affs": [
        0
      ],
      "name": "Kai Yang"
    },
    {
      "affs": [
        2
      ],
      "name": "Yousheng Yan"
    },
    {
      "affs": [
        3
      ],
      "name": "Chenghong Yin",
      "orcid": "0000-0002-2503-3285"
    }
  ],
  "bibtex": "https://research.draconitic.com/paper/1kpcn17y22x00.bib",
  "cited_by": 0,
  "doi": "10.1186/s40246-026-01022-w",
  "fulltext_url": "https://europepmc.org/articles/PMC13721331",
  "id": "1kpcn17y22x00",
  "issns": [
    "1473-9542",
    "1479-7364"
  ],
  "landing_url": "https://europepmc.org/article/MED/42958445",
  "language": "eng",
  "licence": "CC-BY-NC-ND",
  "licence_label": "CC BY-NC-ND",
  "licence_source": "article",
  "licence_url": "https://creativecommons.org/licenses/by-nc-nd/4.0/",
  "metadata_licence": null,
  "native_subjects": [
    [
      "heading",
      "Research"
    ],
    [
      "openalex",
      "2735|Prenatal Screening and Diagnostics"
    ]
  ],
  "openalex": "W7172319216",
  "pdf_url": "https://europepmc.org/articles/PMC13721331?pdf=render",
  "pmcid": "PMC13721331",
  "pmid": "42958445",
  "published": "2026-08-03",
  "publisher": "BMC",
  "ris": "https://research.draconitic.com/paper/1kpcn17y22x00.ris",
  "sources": [
    {
      "first_seen": "2026-11-01T00:20:47Z",
      "native_id": "MED:42958445",
      "source": "europepmc",
      "url": "https://europepmc.org/article/MED/42958445"
    },
    {
      "first_seen": "2026-11-03T12:22:02Z",
      "native_id": "PMC13721331",
      "source": "pmc",
      "url": "https://doi.org/10.1186/s40246-026-01022-w"
    }
  ],
  "subjects": [
    {
      "field": "medicine",
      "origin": "openalex:2735|Prenatal Screening and Diagnostics",
      "subfield": "reproductive-child"
    }
  ],
  "title": "Genetic diagnostic yield of prenatal testing for fetal central nervous system abnormalities: a phenotype-driven study in a large single-center cohort.",
  "title_text": "Genetic diagnostic yield of prenatal testing for fetal central nervous system abnormalities: a phenotype-driven study in a large single-center cohort.",
  "type": "peer-reviewed",
  "updated_at": "2026-11-03T12:22:02Z",
  "url": "https://research.draconitic.com/paper/1kpcn17y22x00",
  "venue": "Human genomics",
  "versions": []
}