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Autor:
T. B. Powles, Jane Evanson, J. E. Drinkwater, Ashley B. Grossman, Piers N. Plowman, Gregory Kaltsas, Paul J. Jenkins, John P Monson, G. M. Besser
Publikováno v:
The Journal of clinical endocrinology and metabolism. 85(4)
Langerhans cell histiocytosis (LCH) is a rare disorder in which granulomatous deposits occur at multiple sites within the body, but which often involves the hypothalamo-pituitary axis (HPA). Although diabetes insipidus (DI) is a well recognized compl