Current Clinical Guidelines for the Management of Patients with Glycogen Storage Disease

Current Clinical Guidelines for the Management of Patients with Glycogen Storage Disease

Glycogen storage disease refers to hereditary pathologies of carbohydrate metabolism, its cause is mutations of various genes encoding enzymes responsible for the synthesis and breakdown of glycogen. Due to enzyme defects, excessive glycogen deposition occurs in cells of various tissues, mainly in t...

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Main Authors: Natalia A. Averkina, Madlena E. Bagaeva, Aleksander A. Baranov, Nato D. Vashakmadze, Elena A. Vishneva, Olga S. Gundobina, Nataliya V. Zhurkova, Elena V. Kaitukova, Elena V. Komarova, Tea V. Margieva, Leyla S. Namazova-Baranova, Valeria P. Novikova, Elena E. Petryaykina, Mariya M. Platonova, Aleksander S. Potapov, Olga Ya. Smirnova, Tatiana V. Strokova, Andrey N. Surkov, Nataliya N. Taran, Marina V. Fedoseenko, Nataliya A. Semenova, Inga V. Anisimova, Svetlana A. Repina, Dmitriy M. Subbotin, Valeria V. Sviridova, Anatoliy I. Havkin, Ekaterina A. Yablokova, Galina V. Volynets, Irina V. Sadovnikova, Elena L. Tumanova
Format: Article
Language:Russian
Published: Union of pediatricians of Russia 2024-07-01
Series:Педиатрическая фармакология
Subjects:
abnormalities in glucose metabolism
glycogen-storage disease
glycogenosis
clinical guidelines
children
Online Access:https://www.pedpharma.ru/jour/article/view/2467
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