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A case of glycogen storage disease type 1a mimicking familial chylomicronemia syndrome Cover

A case of glycogen storage disease type 1a mimicking familial chylomicronemia syndrome

Balkan Journal of Medical Genetics
Volume 24 (2021): Issue 1 (June 2021)
By: A Olgac,  İ Okur,  G Biberoğlu,  FS Ezgü and  L Tümer  
Open Access
|Jul 2021

Authors

A Olgac

mabolgac@yahoo.com

Department of Pediatric Metabolism, Division of Pediatric Metabolism, University of Health Sciences, Dr. Sami Ulus Maternity and Child Health, Training and Research Hospital, Ankara, Turkey

İ Okur

Department of Pediatric Metabolism and Nutrition, Gazi University Hospital, Ankara, Turkey

G Biberoğlu

Department of Pediatric Metabolism and Nutrition, Gazi University Hospital, Ankara, Turkey

FS Ezgü

Department of Pediatric Metabolism and Nutrition, Gazi University Hospital, Ankara, Turkey

L Tümer

Department of Pediatric Metabolism and Nutrition, Gazi University Hospital, Ankara, Turkey
DOI: https://doi.org/10.2478/bjmg-2021-0013 | Journal eISSN: 2199-5761
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Language: English
Page range: 103 - 106
Published on: Jul 27, 2021
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
Keywords:
Familial chylomicronemia syndrome (FCS),
Glycogen storage disease type 1a (GSD1a),
Hypertriglyceridemia (HTG),
Pancreatitis
Related subjects:
Medicine,
Basic medical science,
Basic medical science, other

© 2021 A Olgac, İ Okur, G Biberoğlu, FS Ezgü, L Tümer, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

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