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MON-433 The Spectrum Of Growth Hormone Excess In Carney Complex: Characterizing A Common Finding In A Rare Syndrome

Objective: Carney complex (CNC) is a familial lentiginosis and multiple endocrine neoplasia syndrome, caused by PRKAR1A gene mutations in 70% of patients. Involvement of the pituitary somatotrophs may lead to growth hormone (GH) excess; however, little is published about the progress and management...

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Detaylı Bibliyografya
Yayımlandı:J Endocr Soc
Asıl Yazarlar: Tatsi, Christina, Karageorgiadis, Alexander, Faucz, Fabio, Nikolaos, Settas, Lyssikatos, Charalampos, Elena, Belyavskaya, Lodish, Maya, Stratakis, Constantine
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Endocrine Society 2019
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6550880/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-MON-433
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