Glycogen Storage Disease, Type III (GSD III)

Sponsored diagnostic testing programs for Glycogen Storage Disease, Type III (GSD III)

Glycogen Storage Disease Type III (GSD III) is a rare metabolic disorder caused by impaired glycogen breakdown, leading to excess glycogen in the liver and muscles. Individuals may experience low blood sugar, hepatomegaly, elevated liver enzymes, muscle weakness, and, in some cases, cardiomyopathy. Symptoms often begin in childhood and can vary widely in severity.

1 program found for Glycogen Storage Disease, Type III (GSD III)

Programs

1 program
Invitae Unlock™

Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel

The Invitae Unlock™ Cardiomyopathy & Arrhythmia program offers no-charge genetic testing for U.S. patients with suspected inherited cardiomyopathy or arrhythmia. The comprehensive panel supports diagnostic clarification, risk assessment, and family variant identification. Eligible patients may access testing at no cost when ordered by a qualified healthcare provider.

Cardiology
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Performing labInvitae | Labcorp