Novel homozygous OSGEP gene pathogenic variants in two unrelated patients with Galloway-Mowat syndrome: case report and review of the literature

BMC Nephrol. 2019 Apr 11;20(1):126. doi: 10.1186/s12882-019-1317-y.


Background: Galloway-Mowat syndrome (GAMOS) is a rare autosomal recessive disorder characterized by early-onset nephrotic syndrome and microcephaly with brain anomalies. WDR73 pathogenic variants were described as the first genetic cause of GAMOS and, very recently, four novel causative genes, OSGEP, LAGE3, TP53RK, and TPRKB, have been identified.

Case presentation: We present the clinical and genetic characteristics of two unrelated infants with clinical suspicion of GAMOS who were born from consanguineous parents. Both patients showed a similar clinical presentation, with early-onset nephrotic syndrome, microcephaly, brain atrophy, developmental delay, axial hypotonia, and early fatality. We identified two novel likely disease-causing variants in the OSGEP gene. These two cases, in conjunction with the findings of a literature review, indicate that OSGEP pathogenic variants are associated with an earlier onset of nephrotic syndrome and shorter life expectancy than WDR73 pathogenic variants.

Conclusions: Our findings expand the spectrum of pathogenic variants in the OSGEP gene and, taken in conjunction with the results of the literature review, suggest that the OSGEP gene should be considered the main known monogenic cause of GAMOS. Early genetic diagnosis of GAMOS is of paramount importance for genetic counseling and family planning.

Keywords: Case report; Galloway-Mowat syndrome; Genetic testing; KEOPS complex; Nephrotic syndrome; OSGEP.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Atrophy
  • Biopsy
  • Brain / diagnostic imaging
  • Brain / pathology
  • Clinical Deterioration
  • Fatal Outcome
  • Female
  • Genetic Predisposition to Disease
  • Hernia, Hiatal* / complications
  • Hernia, Hiatal* / diagnosis
  • Hernia, Hiatal* / genetics
  • Hernia, Hiatal* / mortality
  • Homozygote
  • Humans
  • Infant
  • Kidney / pathology*
  • Life Expectancy
  • Male
  • Metalloendopeptidases / genetics*
  • Microcephaly* / complications
  • Microcephaly* / diagnosis
  • Microcephaly* / etiology
  • Microcephaly* / genetics
  • Microcephaly* / mortality
  • Nephrosis* / complications
  • Nephrosis* / diagnosis
  • Nephrosis* / genetics
  • Nephrosis* / mortality
  • Nephrotic Syndrome* / diagnosis
  • Nephrotic Syndrome* / etiology
  • Nephrotic Syndrome* / genetics


  • Metalloendopeptidases
  • O-sialoglycoprotein endopeptidase

Supplementary concepts

  • Galloway Mowat syndrome