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

Stayroula Papailiou

Stayroula Papailiou

Second Department of Paediatrics, Children’s Hospital ‘P. & A. Kyriakou, National and Kapodistrian University of AthensAthens, Greece
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Papailiou, Stayroula
, 
Elpis Athina Vlachopapadopoulou

Elpis Athina Vlachopapadopoulou

Department of Endocrinology, Growth and Development, ‘P. & A. Kyriakou Children’s HospitalAthens, Greece
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Vlachopapadopoulou, Elpis Athina
, 
Amalia Sertedaki

Amalia Sertedaki

Division of Endocrinology, Metabolism and Diabetes, First Department of Pediatrics, National and Kapodistrian University of Athens Medical School, ‘Aghia Sophia’ Children’s HospitalAthens, Greece
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Sertedaki, Amalia
, 
Despoina Maritsi

Despoina Maritsi

Second Department of Paediatrics, Children’s Hospital ‘P. & A. Kyriakou, National and Kapodistrian University of AthensAthens, Greece
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Maritsi, Despoina
, 
Nikolaos Syggelos

Nikolaos Syggelos

Second Department of Paediatrics, Children’s Hospital ‘P. & A. Kyriakou, National and Kapodistrian University of AthensAthens, Greece
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Syggelos, Nikolaos
 and 
Angeliki Syggelou

Angeliki Syggelou

Second Department of Paediatrics, Children’s Hospital ‘P. & A. Kyriakou, National and Kapodistrian University of AthensAthens, Greece
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Syggelou, Angeliki
  
Aug 27, 2020
Aldosterone synthase deficiency type II: an unusual presentation of the first Greek case reported with confirmed genetic analysis's Cover Image
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Published Online: Aug 27, 2020
Page range: 227 - 229
DOI: https://doi.org/10.2478/enr-2020-0025
Keywords
© 2020 Stayroula Papailiou et al., published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
Language:
English
Publication timeframe:
1 times per year
Journal Subjects:
Life Sciences, Molecular Biology, Neurobiology, Medicine, Basic Medical Science, Basic Medical Science, other, Clinical Medicine, Internal Medicine, Endocrinology, Diabetology
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