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Nutrients that Stimulate GLP-1 Secretion (also known as secretagogues) GLP-1 is produced in L cells which are abundant in the lining of the large intestine (Figure 3)

All were non-serious and of mild or moderate severity

Based on the clinical prediction scale, 1 urinary copper levels that are twice the upper limit of normal in the absence of acute hepatitis and serum ceruloplasmin less than 10 mg/dL is highly suggestive of Wilson disease

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The condition progresses slowly, but overall has a good prognosis, if early treatment is begun before organ damage occurs, and if proper treatment plan is adhered to While mental retardation is irreversible if it occurs, most complications of Carnitine Deficiency Syndrome are generally controlled, once prompt and appropriate treatment is provided Additional and Useful Relevant Information for Carnitine Deficiency Syndrome: The following DoveMed website link is a useful resource for additional information:

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