| The collaboration between the Service of Medical Oncology,
which is the one that assists the patients, and the Genetic Counsel
Unit of ICO in Hospitalet have brought about an advance in the identification
of the hereditary tendency to develop a rare syndrome which associates
uterine lomiomes and kidney cancer in the clear cells through the study
of a new mutation of the FH gene. This project has been elaborated
together with the University of Helsinki and published in Human Pathology: “Conventional
renal cancer in a patient with fumarate hydratase mutation (Doi:10.106/j.humpath.2006.10.011) |
