Sponsored diagnostic testing programs for Danon Disease
Danon disease is a rare genetic multisystem disorder caused by pathogenic variants in the LAMP2 gene. It most often presents with hypertrophic cardiomyopathy, skeletal muscle weakness, and learning difficulties. Symptoms typically appear in childhood or adolescence, with males generally experiencing more severe and earlier onset disease than females. Without timely recognition, the cardiac features can progress rapidly, making early diagnosis essential.
2 programs found for Danon Disease
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.
The Mission: Genome – Danon Disease Program offers no-charge Invitae testing for US-based patients with clinical suspicion of Danon disease. Testing includes LAMP2 as part of the Invitae Arrhythmia and Cardiomyopathy Panel. Eligible patients also receive no-charge post-test genetic counseling to support result interpretation and follow-up care.
