Propionic Acidemia

Sponsored diagnostic testing programs for Propionic Acidemia

Propionic Acidemia is a rare inherited metabolic disorder caused by defects in the breakdown of certain amino acids and fats, leading to toxic buildup of propionic acid. Symptoms often begin in infancy and may include poor feeding, vomiting, lethargy, metabolic acidosis, and risk of long-term neurologic and cardiac complications. Early diagnosis and metabolic management are essential for stabilizing patients and preventing severe episodes.

1 program found for Propionic Acidemia

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