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Pediatric Adrenocortical Tumors: What They Can Tell Us on Adrenal Development and Comparison with Adult Adrenal Tumors

Adrenocortical tumors (ACT) in children are very rare and are most frequently diagnosed in the context of the Li-Fraumeni syndrome, a multiple cancer syndrome linked to germline mutations of the tumor suppressor gene TP53 with loss of heterozygosity in the tumors. A peak of children ACT incidence is...

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Bibliografske podrobnosti
izdano v:Front Endocrinol (Lausanne)
Main Authors: Lalli, Enzo, Figueiredo, Bonald C.
Format: Artigo
Jezik:Inglês
Izdano: Frontiers Media S.A. 2015
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4332354/
https://ncbi.nlm.nih.gov/pubmed/25741319
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2015.00023
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