Phakomatoses and Endocrine Gland Tumors: Noteworthy and (Not so) Rare Associations

Phakomatoses encompass a group of rare genetic diseases, such as von Hippel-Lindau syndrome (VHL), neurofibromatosis type 1 (NF1), tuberous sclerosis complex (TSC) and Cowden syndrome (CS). These disorders are due to molecular abnormalities on the RAS-PI3K-Akt-mTOR pathway for NF1, TSC and CS, and t...

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Dettagli Bibliografici
Pubblicato in:Front Endocrinol (Lausanne)
Autori principali: Chevalier, Benjamin, Dupuis, Hippolyte, Jannin, Arnaud, Lemaitre, Madleen, Do Cao, Christine, Cardot-Bauters, Catherine, Espiard, Stéphanie, Vantyghem, Marie Christine
Natura: Artigo
Lingua:Inglês
Pubblicazione: Frontiers Media S.A. 2021
Soggetti:
Endocrinology
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC8134657/
https://ncbi.nlm.nih.gov/pubmed/34025587
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2021.678869
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