Genomic, Proteomic, and Phenotypic Spectrum of Novel O-Sialoglycoprotein Endopeptidase Variant in Four Affected Individuals With Galloway-Mowat Syndrome

Author:

Ali Alghamdi Malak,Benabdelkamel Hicham,Masood Afshan,Saheb Sharif-Askari Narjes,Hachim Mahmood Y.,Alsheikh Hamad,Hamad Muddathir H.,Salih Mustafa A.,Bashiri Fahad A.,Alhasan Khalid,Kashour Tarek,Guatibonza Moreno Pilar,Schröder Sabine,Karageorgou Vasiliki,Bertoli-Avella Aida M.,Alkhalidi Hisham,Jamjoom Dima Z.,Alorainy Ibrahim A.,Alfadda Assim A.,Halwani Rabih

Abstract

Galloway-Mowat syndrome is a rare autosomal recessive disease characterized by a unique combination of renal and neurological manifestations, including early-onset steroid-resistant nephrotic syndrome, microcephaly, psychomotor delay, and gyral abnormalities of the brain. Most patients die during early childhood. Here, we identified a novel homozygous O-sialoglycoprotein endopeptidase (OSGEP) variant, NM_017807.3:c.973C>G (p.Arg325Gly), in four affected individuals in an extended consanguineous family from Saudi Arabia. We have described the detailed clinical characterization, brain imaging results, and muscle biopsy findings. The described phenotype varied from embryonic lethality to early pregnancy loss or death at the age of 9. Renal disease is often the cause of death. Protein modeling of this OSGEP variant confirmed its pathogenicity. In addition, proteomic analysis of the affected patients proposed a link between the KEOPS complex function and human pathology and suggested potential pathogenic mechanisms.

Publisher

Frontiers Media SA

Subject

Genetics (clinical),Genetics,Molecular Medicine

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