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Table of Contents Understanding Exendin-4 and Its Role in Diabetes Treatment What Is Mounjaro and How Does It Differ from Exendin-4

To differentiate SPCD and other mutations in the SLC22A5 gene (as seen in case 2) from alternative causes of carnitine deficiency, a thorough anamnesis and supplementary tests are suggested

C., Yamamoto, L

doi: 10.1111/cns.13694 33 WangZYHanQQDengMYZhaoMJApryaniEShoaibRMet al

Hereditary causes include genetic defects in the metabolism of amino acids, cholesterol, and fatty acids, such as propionyl-CoA carboxylase deficiency (aka propionic acidemia) and medium chain acyl-CoA dehydrogenase deficiency (36)