Aldosterone synthase deficiency type II: an unusual presentation of the first Greek case reported with confirmed genetic analysis
, , , , oraz
27 sie 2020
O artykule
Data publikacji: 27 sie 2020
Zakres stron: 227 - 229
DOI: https://doi.org/10.2478/enr-2020-0025
Słowa kluczowe
© 2020 Stayroula Papailiou et al., published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
Papailiou, Stayroula
Second Department of Paediatrics, Children’s Hospital ‘P. & A. Kyriakou, National and Kapodistrian University of AthensAthens, Greece
Vlachopapadopoulou, Elpis Athina
Department of Endocrinology, Growth and Development, ‘P. & A. Kyriakou Children’s HospitalAthens, Greece
Sertedaki, Amalia
Division of Endocrinology, Metabolism and Diabetes, First Department of Pediatrics, National and Kapodistrian University of Athens Medical School, ‘Aghia Sophia’ Children’s HospitalAthens, Greece
Maritsi, Despoina
Second Department of Paediatrics, Children’s Hospital ‘P. & A. Kyriakou, National and Kapodistrian University of AthensAthens, Greece
Syggelos, Nikolaos
Second Department of Paediatrics, Children’s Hospital ‘P. & A. Kyriakou, National and Kapodistrian University of AthensAthens, Greece
Syggelou, Angeliki
Second Department of Paediatrics, Children’s Hospital ‘P. & A. Kyriakou, National and Kapodistrian University of AthensAthens, Greece