Glycogen Storage Disease (GSD)
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작성자 Arnette Howland 댓글 0건 조회 20회 작성일 25-07-25 14:14본문
What is glycogen storage illness? Glycogen storage diseases (GSDs) are a bunch of uncommon situations by which your body can’t use or store glycogen properly. They’re forms of inherited (passed from mother or father to baby) metabolic disorders. Advertising on our site helps assist our mission. We don't endorse non-Cleveland Clinic products or services. Glycogen is the stored form of glucose (sugar). Glucose is your body’s most important supply of power. It comes from carbohydrates (a macronutrient) in certain foods and fluids you eat. When your physique doesn’t immediately want glucose for vitality, it stores glucose primarily in your skeletal muscles and liver as glycogen for later use. Your physique creates glycogen from glucose via a process known as glycogenesis. When your physique wants extra fuel, it breaks down glycogen for use via a course of referred to as glycogenolysis. Several enzymes are accountable for GlucoGold.net these two processes. Glycogen storage diseases occur once you don’t have a number of of these enzymes. Your body can’t use stored glycogen for energy or maintain regular blood glucose ranges. This could cause a number of points, including frequent symptomatic low blood sugar (hypoglycemia), liver damage and muscle weakness. Researchers know more about some types than others. GSD largely affects your liver or muscles. Some sorts trigger issues in different areas of your body, as effectively. For each sort of GSD, there’s an absence (deficiency) of a sure enzyme involved in glycogen storage or breakdown. Healthcare providers might refer to every kind primarily based on the precise enzyme that’s lacking or the scientist who discovered that sort of GSD. Glycogen storage disease is uncommon. GSD sort I (von Gierke disease), the most common type, occurs in approximately 1 in 100,000 births.
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