A RARE CAUSE OF BOTH HYPO AND HYPERGLYCEMIA; GLYCOGEN STORAGE DISEASE TYPE 0: A CASE REPORT

Year 2021, , 454 - 456, 31.07.2021

Meryem Karaca Halil Aslan

https://doi.org/10.26650/IUITFD.2020.0040

Abstract

Glycogen-storage disease type 0A is a rare autosomal recessively inherited disease resulting from a hepatic glycogen synthase enzyme deficiency. Glycogen-storage disease type 0A is characterized by fasting ketotic hypoglycaemia, postprandial hyperglycemia and lactic acidemia without hepatomegaly. In clinical practice, patients may be asymptomatic, or may present with hypoglycemic convulsions, short stature, growth retardation, osteopenia, and rarely symptoms of hyperglycemia. In this article, we present a 6-year-old girl with previous symptoms of hypoglycaemia, and symptoms of hyperglycemia at the time of admission and genetically diagnosed as glycogen storage disease type 0A.

Keywords

Glycogen storage disease type 0A, ketotic hypoglycaemia, hyperglycaemia, lactic acidemia

HİPO VE HİPERGLİSEMİNİN NADİR BİR NEDENİ; GLİKOJEN DEPO HASTALIĞI TİP 0: OLGU SUNUMU

Abstract

Glikojen depo hastalığı tip 0A; hepatik glikojen sentaz enzim eksikliği sonucu ortaya çıkan otozomal resesif kalıtılan nadir bir hastalıktır. Glikojen depo tip 0A hastalığı hepatomegali olmaksızın açlık ketotik hipoglisemisi, postprandiyal hiperglisemi ve laktik asidemi ile karakterizedir. Klinik pratikte hastalar asemptomatik olabileceği gibi hipoglisemik konvülziyon, boy kısalığı, büyüme geriliği, osteopeni ve seyrek olarak hiperglisemi semptomları ile başvurabilirler. Bu yazıda daha önce hipoglisemi semptomları olan ve başvuru anında hiperglisemi semptomları bulunan postprandiyal laktik asidemi bulguları ile genetik olarak glikojen depo hastalığı tip 0A tanısı konan 6 yaşında kız hasta sunuldu.

Keywords

Glikojen depo hastalığı tip 0A, ketotik hipoglisemi, hiperglisemi, laktik asidemi

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