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March 10, 2026QJM0 citations

OSGEP -Associated Galloway-Mowat Syndrome: A Longitudinal Genotype-Phenotype Correlation from Prenatal Imaging Markers to Lifespan Neurologic-Renal Trajectories

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FLFake LiGuangdong Province Women and Children HospitalYWYunan WangGuangdong Province Women and Children HospitalCYChaoxiang YangGuangdong Province Women and Children Hospital

Key Points

  • To characterize the genetic and phenotypic spectrum of Galloway-Mowat syndrome type 3 and evaluate the correlation of prenatal imaging features with neurological and renal outcomes throughout life.
  • Retrospective review of medical records of genetically diagnosed GAMOS3 cases at a center from January 2016 to August 2024.
  • Systematic review of reported cases in literature to gather additional data.
  • Clinical validity assessment of the gene-disease relationship between OSGEP and GAMOS3.
  • Postnatal renal and neurological dysfunction correlated with prenatal imaging findings, indicating disease progression.
  • Prominent prenatal features included fetal growth restriction (FGR), microcephaly, oligohydramnios, and abnormal cranial imaging.
  • FGR worsened with gestation, primarily affecting the fetal head and abdomen while sparing long bones.
  • Trio-based medical exome sequencing identified novel variants in the OSGEP gene, expanding the genetic spectrum of GAMOS3.
  • The OSGEP gene-disease relationship was validated as 'Definitive' according to clinical-genetic standards.

Abstract

Abstract Background Galloway-Mowat syndrome type 3 (GAMOS3) is a rare autosomal recessive disorder characterized by the co-occurrence of renal and neurological abnormalities in early childhood, caused by OSGEP gene variants. Aim This study aims to characterize the genetic and phenotypic spectrum of GAMOS3 and evaluate correlations from prenatal imaging features to lifelong neurological and renal manifestations. Method We retrospectively reviewed the medical records of cases genetically diagnosed with OSGEP-associated GAMOS3 at our center between January 2016 and August 2024. Additionally, a systematic review of reported cases in literature was conducted. The clinical validity of the gene-disease relationship between OSGEP and GAMOS3 was also evaluated in accordance with the ClinGen Gene-Disease Clinical Validity Curation Framework. Results The postnatal renal and neurological dysfunction was associated with prenatal manifestations, indicating disease progression. Prominent prenatal features included fetal growth restriction (FGR), microcephaly, oligohydramnios, and abnormal cranial imaging. Notably, FGR worsened with advancing gestation, predominantly affecting fetal head and abdominal growth while sparing long bones. Fetal central nervous system magnetic resonance imaging revealed uncommon findings such as abnormal sulcation and increased T2 signal in the white matter, suggestive of myelination defects or leukoencephalopathy. Trio-based medical exome sequencing identified novel variants in the OSGEP gene within this cohort, expanding the known genetic spectrum of GAMOS3. Furthermore, the gene-disease relationship between OSGEP and GAMOS3 was conclusively validated as “Definitive” according to clinical-genetic criteria. Conclusions This study provides a comprehensive overview of the clinical phenotypes and genetic spectrum of GAMOS3, spanning from the prenatal period throughout the life course.

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Cite This Study

Li et al. (2026) studied this question.

synapsesocial.com/papers/69af952b70916d39fea4c633https://doi.org/10.1093/qjmed/hcaf309
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Galloway–Mowat Syndrome Type 3 Caused by OSGEP Gene Variants: A Case Report and Literature Review2022 · 9 citations
  2. 2High positive predictive value of CNVs detected by clinical exome sequencing in suspected genetic diseases2024 · 9 citations
  3. 3Galloway-mowat syndrome 3 (GAMOS3): a novel disease-causing variant in OSGEP gene and expansion of the clinical spectrum2024 · 3 citations
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