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Description
Primary carnitine deficiency (PCD) Primary carnitine deficiency (PCD) is a rare, autosomal recessively inherited congenital disorder (frequency of 1 per 100,000 cases worldwide)
It delivers a clinically effective L Carnitine dosage that supports fat metabolism, energy production, and post-exercise recovery
Aceyl L-Carnitine facilitates the metabolism of fatty acids for energy generation
L-carnitine modulates epileptic seizures in pentylenetetrazole-kindled rats via suppression of apoptosis and Autophagy and Upregulation of Hsp70
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