Mar 13, 2023 · Undoubtedly, the German Shepherd Dog (GSD) is one of the most desired breeds out there. Its intelligence, usefulness, and overall charm can surely woo anyone. But did you know there are many types of German Shepherd Dogs? All in all, there are 14 types of German Shepherds according to their bloodlines, coats, and sizes:

Jun 26, 2023 · Glycogen storage diseases are a group of rare inherited conditions that can cause frequent low blood sugar, muscle weakness and liver damage. There are several different types based on which enzyme is missing, and each one affects you differently. Most types are manageable with treatment. What is glycogen storage disease?

A glycogen storage disease (GSD, also glycogenosis and dextrinosis) is a metabolic disorder caused by a deficiency of an enzyme or transport protein affecting glycogen synthesis, glycogen breakdown, or glucose breakdown, typically in muscles and/or liver cells. [1] GSD has two classes of cause: genetic and environmental.

Experts know of at least 9 types of GSD. They are grouped by the enzyme that is missing in each one. Each GSD has its own symptoms and needs different treatment. The most common types of GSD are types I, III, and IV: Type I or von Gierke disease. This is the most common form of GSD.

Jan 21, 2025 · Glycogen storage diseases (GSDs), also known as glycogenoses, are inherited inborn errors of carbohydrate metabolism. GSDs may manifest at any age, from neonatal life to adulthood.

The most common types of GSD are types I, II, III and IV, accounting for nearly 90% of all cases. About 25% of patients with GSD are thought to have type I. GSD types VI and IX can have very mild symptoms and may be underdiagnosed or not diagnosed until adulthood.

Dec 23, 2024 · Glycogen storage disease (GSD) refers to a group of rare genetic conditions that affect how the body stores and breaks down glycogen. The most common type is type I, also called von Gierke...

Apr 12, 2023 · What are the types of glycogen storage disease? There are many types of GSD, some of which are further divided into subtypes. The most common types are types 1 and 3. GSD type 1, also called Von Gierke disease, is caused by mutations in the G6PC or SLC37A4 genes.

Glycogen storage disease (GSD) also known as glycogenoses is a diverse group of rare inherited metabolic disorders (there are over 20 types of glycogen storage disease including the subtypes) involving inherited defect in one of the enzymes responsible for forming glycogen, or for releasing glucose from glycogen as it is needed by your body ...

There are over 20 types of GSD including the subtypes. This heterogeneous group of rare diseases represents inborn errors of carbohydrate metabolism and are classified based on the deficient enzyme and affected tissues. GSDs primarily affect liver or muscle or both as glycogen is particularly abundant in these tissues.