A CASE OF ATYPICAL SYSTEMIC PRIMARY CARNITINE DEFICIENCY IN SAUDI ARABIA

Systemic primary carnitine deficiency (SPCD) is an autosomal recessive inborn error of fatty acid metabolism caused by a defect in the transporter responsible for Headlights moving carnitine across plasma membrane.The clinical features of SPCD vary widely based on the age of onset and organs involved.During infancy, patients might show episodes of

Abstract As globalization increases the interconnectedness between nations, economies, and industries, the introduction of diseases will continue to remain a prominent threat to the livestock sector and the trade of animals and animal Dolls Stroller products, as well as the livelihoods of farmers, food security and public health.The global pig sect