New mutation in WT1 gene in a boy with an incomplete form of Denys-Drash syndrome: A CARE-compliant case report

RATIONALE: Pediatric patients with WTl-associated syndromes (including Wilms’ tumor-aniridia syndrome and Denys-Drash syndrome), Perlman syndrome, mosaic aneuploidy, and Fanconi anemia with a biallelic breast cancer type 2 susceptibility protein mutation have the highest risk of developing Wilms’ tu...

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Detalles Bibliográficos
Autores principales: Akramov, Nail R., Shavaliev, Rafael F., Osipova, Ilsiya V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
6200
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8133155/
https://www.ncbi.nlm.nih.gov/pubmed/34106634
http://dx.doi.org/10.1097/MD.0000000000025864

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8133155/
https://www.ncbi.nlm.nih.gov/pubmed/34106634
http://dx.doi.org/10.1097/MD.0000000000025864

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