Gonadal Function in 15 Patients Associated with WT1 Gene Mutations

Denys-Drash syndrome (DDS) and Frasier syndrome (FS) are caused by mutations of the WT1 gene. These disorders are characterized by renal disease, abnormality of male sex differentiation, and Wilms’ tumor and gonadoblastoma. There have been few reports on gonadal function in a large series of patient...

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Detalles Bibliográficos
Autores principales: Maesaka, Akiko, Higuchi, Asako, Kotoh, Shinobu, Hasegawa, Yukihiro, Ikeda, Masahiro, Shishido, Seiichirou, Honda, Masataka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society for Pediatric Endocrinology 2006
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4004866/
https://www.ncbi.nlm.nih.gov/pubmed/24790335
http://dx.doi.org/10.1297/cpe.15.143

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4004866/
https://www.ncbi.nlm.nih.gov/pubmed/24790335
http://dx.doi.org/10.1297/cpe.15.143

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