Sponsored diagnostic testing programs for SDHA-related Mitochondrial Complex II Deficiency
SDHA-related Mitochondrial Complex II Deficiency is a rare genetic disorder caused by pathogenic variants in the SDHA gene, leading to impaired mitochondrial energy production. Affected individuals may experience muscle weakness, exercise intolerance, developmental delay, neurologic symptoms, or organ system involvement depending on severity. Because presentations vary widely, genetic testing is an important tool for confirming the diagnosis and guiding clinical management.
1 program found for SDHA-related Mitochondrial Complex II Deficiency
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.
