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

• Main Authors: Natalia A. Averkina (Author), Madlena E. Bagaeva (Author), Aleksander A. Baranov (Author), Nato D. Vashakmadze (Author), Elena A. Vishneva (Author), Olga S. Gundobina (Author), Nataliya V. Zhurkova (Author), Elena V. Kaitukova (Author), Elena V. Komarova (Author), Tea V. Margieva (Author), Leyla S. Namazova-Baranova (Author), Valeria P. Novikova (Author), Elena E. Petryaykina (Author), Mariya M. Platonova (Author), Aleksander S. Potapov (Author), Olga Ya. Smirnova (Author), Tatiana V. Strokova (Author), Andrey N. Surkov (Author), Nataliya N. Taran (Author), Marina V. Fedoseenko (Author), Nataliya A. Semenova (Author), Inga V. Anisimova (Author), Svetlana A. Repina (Author), Dmitriy M. Subbotin (Author), Valeria V. Sviridova (Author), Anatoliy I. Havkin (Author), Ekaterina A. Yablokova (Author), Galina V. Volynets (Author), Irina V. Sadovnikova (Author), Elena L. Tumanova (Author)
• Format: Book
• Published: Union of pediatricians of Russia, 2024-07-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

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...