Familial <i>WT1</i> -associated nephropathy - 46, XY Frasier syndrome and 46, XX steroid-resistant nephrotic syndrome in female siblings: A case report and review of literature
Despite identical mutations, phenotypic differences highlight complex genotype-phenotype relations, stressing the need for research, genetic counseling, and family member screening.
Authors
- Mahipal Khandelwal
- Kiran G Piparva
- Deepak Parchwani
Institutions
- Gujarat Kidney Foundation (IN)
- All India Institute of Medical Sciences (IN)
Publication Details
- Journal
- World Journal of Nephrology
- Published
- 2026-03-13
- DOI
- https://doi.org/10.5527/wjn.v15.i1.110867
- Primary Topic
- Renal and related cancers
- Type
- article
- Field-Weighted Citation Impact
- 0.00