A clinical case of glycogen disease type III in a child
https://doi.org/10.25789/YMJ.2023.84.32
Abstract
Glycogenosis type III (Cori disease) is one of the most common glycogen storage diseases in the world. The disease is associated with a disorder of carbohydrate metabolism: glycogen metabolism, leading to disruption of its synthesis or breakdown and is characterized by excessive accumulation of this polysaccharide in the organs and tissues of the body, most often in the liver or muscles. This article presents a clinical case of glycogen storage disease type III.
Keywords
About the Authors
V. B. EgorovaRussian Federation
Egorova Vera Borisovna – Candidate of Medical Sciences, Associate Professor of the Department of Pediatrics and Pediatric Surgery
T. E. Burtseva
Russian Federation
Burtseva Tatyana Egorovna – Doctor of Medical
Sciences, Professor of the Department of Pediatrics and Pediatric Surgery; head of lab.
Ya. A. Munkhalova
Russian Federation
Munkhalova Yana Afanasyevna – Candidate of Medical Sciences, Head of the Department of Pediatrics and Pediatric Surgery
N. N. Innokentyeva
Russian Federation
Innokentyeva Natalya Nikolaevna – doctor of the gastroenterology department of the Pediatric Center
M. V. Khandy
Russian Federation
Khandy Maria Vasilienva – Doctor of Medical Sciences, Professor of the Department of Propaedeutics of Children Diseases
M. A. Sharina
Russian Federation
Sharina Maria Antoninovna – resident of the Department of Pediatrics and Pediatric Surgery
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Review
For citations:
Egorova V.B., Burtseva T.E., Munkhalova Ya.A., Innokentyeva N.N., Khandy M.V., Sharina M.A. A clinical case of glycogen disease type III in a child. Yakut Medical Journal. 2023;(4):137-139. https://doi.org/10.25789/YMJ.2023.84.32