Glycogen storage disease type III screening
Glycogen storage disease type III Microchapters |
Differentiating Glycogen storage disease type III from other Diseases |
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Glycogen storage disease type III screening On the Web |
American Roentgen Ray Society Images of Glycogen storage disease type III screening |
Risk calculators and risk factors for Glycogen storage disease type III screening |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
Glycogen storage disease type 3 is an autosomal recessive disease so carrier screening of at-risk relatives may be done. Screening requires prior identification of AGL pathogenic variants in the family.
Screening
- Glycogen storage disease type 3 is an autosomal recessive disease.
- Carrier screening of at-risk relatives may be done.
- Screening requires prior identification of AGL pathogenic variants in the family.