WT1 complete gonadal dysgenesis with membranoproliferative glomerulonephritis: case series and literature review

BACKGROUND: Intronic WT1 mutations are usually causative of Frasier syndrome with focal segmental glomerulosclerosis as the characteristic nephropathy. Membranoproliferative glomerulonephritis is not commonly associated with disorders of sex development but has been recently identified as a WT1-asso...

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Detalles Bibliográficos
Autores principales: Anderson, Erin, Aldridge, Melanie, Turner, Ross, Harraway, James, McManus, Sam, Stewart, Anna, Borzi, Peter, Trnka, Peter, Burke, John, Coman, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9395477/
https://www.ncbi.nlm.nih.gov/pubmed/35211794
http://dx.doi.org/10.1007/s00467-022-05421-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9395477/
https://www.ncbi.nlm.nih.gov/pubmed/35211794
http://dx.doi.org/10.1007/s00467-022-05421-8

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