2. 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)

3. 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)

4. 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)

5. 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

6. 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

7. 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

8. Glycogen storage disease type 2
Pompe disease; Acid maltase deficiency disease; Aglucosidase alfa; Alpha-1,4-glucosidase deficiency; Cardiomegalia glycogenica diffusa; Deficiency of alpha-glucosidase; GSD II; Deficiency of lysosomal alpha-glucosidase;
rarediseases.info.nih.gov

9. Glycogen storage disease type 5
GSD 5; McArdle disease; McArdle type glycogen storage disease; PYGM deficiency; Muscle glycogen phosphorylase deficiency; Myophosphorylase deficiency;
www.rarediseases.info.nih.gov

10. Sumer's Radiology Site: Interesting abstract-Renal sonographic findings of type I glycogen storage disease in infancy and early childhood.
Background: Type I glycogen storage disease (GSD-I) is an inherited disorder affecting glycogenolysis and gluconeogenesis. The characteristic manifestations are hepatomegaly, hypoglycemia, hyperlacticacidemia,...
sumerdoc.blogspot.com