Rapidly Progressing to ESRD in an Individual with Coexisting ADPKD and Masked Klinefelter and Gitelman Syndromes

• Published in: Genes 2022-02, Vol.13 (3), p.394
• Main Authors: Peces, Ramón, Peces, Carlos, Mena, Rocío, Cuesta, Emilio, García-Santiago, Fe Amalia, Ossorio, Marta, Afonso, Sara, Lapunzina, Pablo, Nevado, Julián
• Format: Article
• Language: English
• Subjects: Aneurysms; Blood pressure; Cardiovascular diseases; Coexistence; Creatinine; Cystic fibrosis; Cysts; Cytogenetics; End-stage renal disease; Families & family life; Genes; Genetic disorders; Genomes; Genomics; Gitelman Syndrome - complications; Gitelman Syndrome - diagnosis; Gitelman Syndrome - genetics; Hereditary diseases; Hernias; Humans; Hypocalciuria; Hypogonadism; Hypokalemia; Hypomagnesemia; Infertility; Karyotypes; Kidney - pathology; Kidney diseases; Kidney Failure, Chronic - genetics; Klinefelter's syndrome; Magnetic resonance imaging; Male; Metabolism; Mitral valve prolapse; Mutation; Patients; Polycystic kidney; Polycystic Kidney, Autosomal Dominant - complications; Polycystic Kidney, Autosomal Dominant - genetics; Polycystic Kidney, Autosomal Dominant - pathology; Renal failure; Renal function; Renal Insufficiency, Chronic; Software; Solute Carrier Family 12, Member 3 - genetics; Y chromosomes
• ISSN: 2073-4425; 2073-4425
• DOI: 10.3390/genes13030394

Autosomal dominant polycystic kidney disease (ADPKD) is the most common monogenetic hereditary renal disease, promoting end-stage renal disease (ESRD). Klinefelter syndrome (KS) is a consequence of an extra copy of the X chromosome in males. Main symptoms in KS include hypogonadism, tall stature, azoospermia, and a risk of cardiovascular diseases, among others. Gitelman syndrome (GS) is an autosomal recessive disorder caused by SLC12A3 variants, and is associated with hypokalemia, hypomagnesemia, hypocalciuria, normal or low blood pressure, and salt loss. The three disorders have distinct and well-delineated clinical, biochemical, and genetic findings. We here report a male patient with ADPKD who developed early chronic renal failure leading to ESRD, presenting with an intracranial aneurysm and infertility. NGS identified two de novo PKD1 variants, one known (likely pathogenic), and a previously unreported variant of uncertain significance, together with two SLC12A3 pathogenic variants. In addition, cytogenetic analysis showed a 47, XXY karyotype. We investigated the putative impact of this rare association by analyzing possible clinical, biochemical, and/or genetic interactions and by comparing the evolution of renal size and function in the proband with three age-matched ADPKD (by variants in PKD1) cohorts. We hypothesize that the coexistence of these three genetic disorders may act as modifiers with possible synergistic actions that could lead, in our patient, to a rapid ADPKD progression.