Glycogen storage disease type III

Inheritance

How is glycogen storage disease type 3 inherited?

Glycogen storage disease type III (GSD III) is an autosomal recessive disorder. This means people with GSD III have genetic changes on both copies of their AGL gene. If you have a child with GSD III, that means both you and your partner are “carriers” for this condition. Carriers of a genetic condition do not have GSD III themselves, but can pass it on to their children. When two carriers of GSD III have children, there is a 1 in 4, or 25% chance for each pregnancy to have GSD III, and a 3 in 4, or 75% chance the child will not have GSD III. Speaking with a genetic counselor, a health professional who specializes in genetic conditions, can help people to understand the chance to have a child with GSD III. To find a genetic counselor near you, use the "find a genetic counselor" tool at the National Society of Genetic Counselors website

References
  • http://ghr.nlm.nih.gov/condition/glycogen-storage-disease-type-iii
  • Dagli A, Sentner CP, Weinstein DA. Glycogen Storage Disease Type III. 2010 Mar 9 [Updated 2012 Sep 6]. In: Pagon RA, Adam MP, Ardinger HH, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2016. Available from: http://www.ncbi.nlm.nih.gov/books/NBK26372/

More Inheritance Content

We use cookies to ensure that we give you the best experience on our website. By continuing to browse this site, you are agreeing to our use of cookies.

Continue Find out more about our use of cookies and similar technology

This content comes from a hidden element on this page.

The inline option preserves bound JavaScript events and changes, and it puts the content back where it came from when it is closed.

Remember Me