An inherited disorder that prevents carnitine from normally attaching to long-chain fatty acids that is used to make energy in the mitochondria. Mutations in the CPT1A gene severely reduce or eliminate the activity of this enzyme.
Register for a membership with Paddle For Kids to join the growing community of support for education of early childhood disorders.
Your donation will go towards the cause of identifying early childhood disorders so that disorders can be treated in a timely manner.
Paddle For Kids is a 501c3 non-profit organization who raises awareness for newborn screenings & programs created for identifying early childhood disorders.