Cantu Syndrome

Sponsored diagnostic testing programs for Cantu Syndrome

Cantu syndrome is a rare genetic disorder characterized by congenital hypertrichosis, distinctive facial features, skeletal overgrowth, and cardiovascular abnormalities such as cardiomegaly and vascular dilation. Caused most often by variants in the ABCC9 or KCNJ8 genes, it presents in infancy or early childhood and requires multidisciplinary management across cardiac, musculoskeletal, and developmental domains.

1 program found for Cantu Syndrome

Programs

1 program
Invitae Unlock™

Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel

The Invitae Unlock™ Cardiomyopathy & Arrhythmia program offers sponsored genetic testing for U.S. patients with suspected inherited cardiomyopathy or arrhythmia. The comprehensive panel supports diagnostic clarification, risk assessment, and family variant identification. The test is billed to insurance first; when a claim is denied or the patient is uninsured, the program's sponsor covers the cost of testing. Testing must be ordered by a qualified healthcare provider.

Cardiology
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Performing lab
Invitae | Labcorp