Familial WT1-associated nephropathy - 46, XY Frasier syndrome and 46, XX steroid-resistant nephrotic syndrome in female siblings: A case report and review of literature.
AI interpretation is pending for this paper.
Open original publication →What the AI sees
Not AI summarized yet.
Research significance
Pending deeper interpretation.
Source abstract
BACKGROUND: The Wilms tumor 1 (WT1) mutation is significantly associated with steroid-resistant nephrotic syndrome (SRNS) in children. It causes a spectrum of disorders, including Frasier and Denys-Drash syndromes. The WT1 gene encodes a transcription factor essential for renal, gonadal, and mesothelial development. The prevalence of Frasier syndrome is 1 in 1000000. Frasier syndrome presents with childhood onset of SRNS, progressing to end-stage kidney disease, has an XY female phenotype, delayed puberty, and gonadal tumor risk. Two siblings with identical WT1 mutations but differing phenotypes offer important clinical insights. CASE SUMMARY: We report a rare familial occurrence of shared mutation of WT1 (at intron 9 splice site: C.1432+5G>A) and COL4A5 genes in two siblings. The elder sibling (46, XY) presented with infantile steroid-resistant nephrotic syndrome and rapidly deteriorating and progressing to end-stage kidney disease with XY karyotype. The genetic testing confirmed the diagnosis of Frasier syndrome associated with a WT1 mutation in the elder sibling. She is currently on maintenance dialysis, awaiting renal transplantation. The younger sibling presented at age four with facial edema and SRNS with slower disease progression and no apparent gonadal anomalies. Her renal biopsy revealed minimal change disease, and she maintains stable renal function under antiproteinuric therapy. Genetic testing confirmed the diagnosis of WT1 mutation with 46, XX karyotype in the younger sibling. Both siblings also carried a COL4A5 gene variant of uncertain significance. Family history reveals consanguineous marriage and a similar presentation in a sibling. CONCLUSION: Despite identical mutations, phenotypic differences highlight complex genotype-phenotype relations, stressing the need for research, genetic counseling, and family member screening.