Aldosterone synthase deficiency type II: an unusual presentation of the first Greek case reported with confirmed genetic analysis
Authors
Stayroula Papailiou
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
Language: English
Page range: 227 - 229
Published on: Aug 27, 2020
In partnership with: Paradigm Publishing Services
Publication frequency: 1 issue per year
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© 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.