fig1

Novel imaging technologies for genetic diagnoses in the inborn errors of metabolism

Figure 1. Demonstration of normal 1H MRS (A); there is an absent creatine peak (arrow, second panel). The first panel shows the normal creatine peak (B); and Sjogren Larsson syndrome demonstrating a prominent lipid peak (C). Adapted from Mano et al.[50]. Lac/lipid: lactate and lipid peaks; NAA: N-acetylaspartate; Glu/Gln: glutamate and glutamine; Cr/PCr: creatine and phosphocreatine; cho: choline; mI: myoinositol

Journal of Translational Genetics and Genomics
ISSN 2578-5281 (Online)
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