Aldosterone synthase deficiency type II: an unusual presentation of the first Greek case reported with confirmed genetic analysis
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27 ago 2020
INFORMAZIONI SU QUESTO ARTICOLO
Pubblicato online: 27 ago 2020
Pagine: 227 - 229
DOI: https://doi.org/10.2478/enr-2020-0025
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© 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