Polyuria-Polydipsia—First Sign of a Rare Hematological Disease
1 Department of Endocrinology, Ploiesti Pediatric Hospital, 100336 Ploiesti, Romania
2 Department of Endocrinology, Diabetes and Metabolic Disorders, Elias University Hospital, 011461 Bucharest, Romania; (L.C.); (S.F.)
3 Department of Endocrnology II, Carol Davila University of Medicine and Pharmacy, 020021 Bucharest, Romania
4 Department of Pediatric Oncology, Department of Pediatric, Marie Curie Emergency Children Hospital, 077120 Bucharest, Romania;
5 Department of Neurosurgery, Department of Pediatric, Marie Curie Emergency Children Hospital, 077120 Bucharest, Romania;
6 Department of Patology, Department of Pediatric, Marie Curie Emergency Children Hospital, 077120 Bucharest, Romania;
7 Department of Pediatric II, Fundeni Clinical Insitute, 022328 Bucharest, Romania;
* Corresponding author:
* Author to whom correspondence should be addressed.
(this article belongs to the Special Issue ENDOPED International Congress 2020)
Received: 26 Oct 2020 / Accepted: 14 Nov 2020 / Published: 17 Nov 2020
Keywords: Langerhans cell histiocytosis; children; diabetes insipidus
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CITE
Vasilache, S.L.; Cima, L.; Fica, S.; Sfrijan, D.; Sorin, T.; Ultimescu, F.; Coliţă, A. Polyuria-Polydipsia—First Sign of a Rare Hematological Disease. CEACR 2020, 2, 52.
Vasilache SL, Cima L, Fica S, Sfrijan D, Sorin T, Ultimescu F, Coliţă A. Polyuria-Polydipsia—First Sign of a Rare Hematological Disease. Central European Annals of Clinical Research. 2020; 2(1):52.
Vasilache, Simona Loredana; Cima, Luminiţa; Fica, Simona; Sfrijan, Doiniţa; Sorin, Târnăveanu; Ultimescu, Flavia; Coliţă, Anca. 2020. "Polyuria-Polydipsia—First Sign of a Rare Hematological Disease." CEACR 2, no. 1: 52.
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