Have a personal or library account? Click to login
Aldosterone synthase deficiency type II: an unusual presentation of the first Greek case reported with confirmed genetic analysis Cover

Aldosterone synthase deficiency type II: an unusual presentation of the first Greek case reported with confirmed genetic analysis

Open Access
|Aug 2020

Authors

Stayroula Papailiou

valia.papailiou@gmail.com

Second Department of Paediatrics, Children’s Hospital ‘P. & A. Kyriakou, National and Kapodistrian University of Athens, Athens, Greece

Elpis Athina Vlachopapadopoulou

Department of Endocrinology, Growth and Development, ‘P. & A. Kyriakou Children’s Hospital, Athens, Greece

Amalia Sertedaki

Division of Endocrinology, Metabolism and Diabetes, First Department of Pediatrics, National and Kapodistrian University of Athens Medical School, ‘Aghia Sophia’ Children’s Hospital, Athens, Greece

Despoina Maritsi

Second Department of Paediatrics, Children’s Hospital ‘P. & A. Kyriakou, National and Kapodistrian University of Athens, Athens, Greece

Nikolaos Syggelos

Second Department of Paediatrics, Children’s Hospital ‘P. & A. Kyriakou, National and Kapodistrian University of Athens, Athens, Greece

Angeliki Syggelou

Second Department of Paediatrics, Children’s Hospital ‘P. & A. Kyriakou, National and Kapodistrian University of Athens, Athens, Greece
DOI: https://doi.org/10.2478/enr-2020-0025 | Journal eISSN: 1336-0329 | Journal ISSN: 1210-0668
Language: English
Page range: 227 - 229
Published on: Aug 27, 2020
Published by: Slovak Academy of Sciences, Institute of Experimental Endocrinology
In partnership with: Paradigm Publishing Services
Publication frequency: 1 issue per year

© 2020 Stayroula Papailiou, Elpis Athina Vlachopapadopoulou, Amalia Sertedaki, Despoina Maritsi, Nikolaos Syggelos, Angeliki Syggelou, published by Slovak Academy of Sciences, Institute of Experimental Endocrinology
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.