| Literature DB >> 26763419 |
Hassan Vahidnezhad1, Leila Youssefian2, Jouni Uitto3.
Abstract
A number of critical signaling pathways are required for homeostatic regulation of cell survival, differentiation, and proliferation during organogenesis. One of them is the PI3K-AKT-mTOR pathway consisting of a cascade of inhibitor/activator molecules. Recently, a number of heritable diseases with skin involvement, manifesting particularly with tissue overgrowth, have been shown to result from mutations in the genes in the PI3K-AKT-mTOR and interacting intracellular pathways. Many of these conditions represent an overlapping spectrum of phenotypic manifestations forming a basis for novel, unifying classifications. Identification of the mutant genes and specific mutations in these patients has implications for diagnostics and genetic counseling and provides a rational basis for the development of novel treatment modalities for this currently intractable group of disorders.Entities:
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Year: 2016 PMID: 26763419 DOI: 10.1038/JID.2015.331
Source DB: PubMed Journal: J Invest Dermatol ISSN: 0022-202X Impact factor: 8.551