A Non-Hereditary Case of Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome

Hereditary leiomyomatosis and renal cell carcinoma (HLRCC) syndrome is believed to result from an autosomal dominant mutation in the fumarate hydratase (FH) gene on chromosome 1. It is characterized by leiomyomas, mainly uterine or cutaneous, and renal cell carcinoma (RCC). The most common type of R...

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Detalles Bibliográficos
Autores principales: Kapila, Vaishali, Kalra, Arjun G, Stockman, David L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7968348/
https://www.ncbi.nlm.nih.gov/pubmed/33747650
http://dx.doi.org/10.7759/cureus.13344

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7968348/
https://www.ncbi.nlm.nih.gov/pubmed/33747650
http://dx.doi.org/10.7759/cureus.13344

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