SAT-444 Pituitary Function and the Response to GH Replacement Therapy in Patients with Histiocytosis: Analysis of the Pfizer International Metabolic Database (KIMS)

Introduction: Langerhans Cell Histiocytosis (LCH) is a rare infiltrative disease with granulomatous deposits sometimes involving the hypothalamus-pituitary axis, with endocrine manifestations that includes diabetes insipidus (DI) and growth hormone deficiency (GHD) as the most prevalent consequences...

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Pubblicato in:J Endocr Soc
Autori principali: Touraine, Philippe, Mattsson, Anders, Burman, Pia, Van Beek, Andre, Aydin, Ferah, Kelepouris, Nicky, Feldt-Rasmussen, Ulla, Camacho-Hubner, Cecilia
Natura: Artigo
Lingua:Inglês
Pubblicazione: Endocrine Society 2019
Soggetti:
Neuroendocrinology and Pituitary
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6552372/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-SAT-444
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