Sponsored diagnostic testing programs for Dystrophy-Dystroglycanopathy Types A4, B4, C4, A5, B5 and C5
Dystrophy-dystroglycanopathies (types A4, B4, C4, A5, B5, and C5) are a group of inherited muscular dystrophies caused by defects in dystroglycan glycosylation. These conditions range from congenital-onset weakness with structural brain and eye involvement to later-onset limb-girdle patterns of muscle disease. Severity varies widely, but all forms involve progressive muscle impairment.
1 program found for Dystrophy-Dystroglycanopathy Types A4, B4, C4, A5, B5 and C5
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.
