Papillary thyroid carcinoma in a boy with familial tuberous sclerosis complex attributable to a TSC2 deletion&mdash

Autor:	Flader, M., Kurzawa, P., Maldyk, J., Sygut, J., Harasymczuk, J., Kropinska, A., Handkiewicz-Junak, D., Jarzab, B., Kotulska, K., Niedziela, M.
Jazyk:	angličtina
Rok vydání:	2017
Předmět:	congenital hereditary and neonatal diseases and abnormalities fungi thyroid cancer food and beverages tuberous sclerosis neoplasms Children nervous system diseases
Zdroj:	Current Oncology Volume 24 Issue 5 Pages 3555-428
ISSN:	1718-7729
DOI:	10.3747/co.24.3555
Popis:	Tuberous sclerosis complex (tsc), a phacomatosis, is a rare genetic disease (autosomal dominant incidence: 1 in 6,800&ndash 17,300) associated with mutations in the TSC1 and TSC2 genes, 70% of which are sporadic. The disease causes benign tumours in the brain, kidneys, heart, lungs, skin, and eyes thyroid lesions are extremely rare.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=multidiscipl::dde6753fe79feb484c6311963fe24b90 Zobrazit plný text záznamu Plný text ve formátu PDF