2. Glycogen Storage Diseases
Glycogen serves as the primary fuel reserve for the body's energy needs. Glycogen storage diseases, also known as glycogenoses, are genetically linked metabolic disorders that involve the enzymes regulating ...
Healthline.com (OMS Preferred Provider)

3. Glycogen storage disease type V - Genetics Home Reference
Glycogen storage disease type V (also known as GSDV or McArdle disease) is an inherited disorder caused by an inability to break down a complex sugar called glycogen in muscle cells. A lack of ...
MedlinePlus (Offsite)

4. Glycogen Storage Disease Type VI -- GeneReviews -- NCBI Bookshelf
by either a US CLIA-licensed laboratory or a non-US clinical laboratory. GeneTests does not verify laboratory-submitted information or warrant any aspect of a laboratory's licensure or performance. Clinicians must communicate directly with the lab...
MedlinePlus (Offsite)

5. Glycogen storage disease type V - References - Genetics Home Reference
These sources were used to develop the Genetics Home Reference condition summary on glycogen storage disease type V.
MedlinePlus (Offsite)

6. Dentin Dysplasia, Type I
Dentin dysplasia type I is an inherited disorder characterized by atypical development of the "dentin" of a person's teeth. Dentin makes up most of the tooth and is the bone-like material under the enamel. It serves to contain the pulp of the toot...
Healthline.com (OMS Preferred Provider)

7. Cholesteryl ester storage disease - Genetics Home Reference
Cholesteryl ester storage disease is a rare inherited condition involving the breakdown and use of fats and cholesterol in the body (lipid metabolism). In affected individuals, harmful amounts of lipids accumulate in cells and tissues throughout t...
MedlinePlus (Offsite)

8. Glycogen Storage Disease Type I - Caring4Cancer
It is possible that the main title of the report Glycogen Storage Disease Type I is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.
www.caring4cancer.com

9. Glycogen-Storage Disease Type I: eMedicine Pediatrics: Genetics and Metabolic Disease
In 1929, von Gierke provided the initial description of glycogen-storage disease type I (GSD I) from autopsy reports of 2 children whose large livers contained excessive glycogen. He also reported similar findings...
emedicine.medscape.com

10. American Liver Foundation - Type I Glycogen Storage Disease
Explore this section to learn more about Type I Glycogen Storage Disease, including a description of the disease and how it's diagnosed.
www.liverfoundation.org