What is phenylketonuria? Discuss its occurrence, symptoms if any, treatments if there are, and any prohibitions in the diet
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- Create or design a concept map explaining in one page using figures, illustrations, and a few descriptions or explanations of the assigned glycogen storage and lipid diseases in your group. The content of your concept map should include the biochemical and molecular basis of the type 0 glycogen storage disease with clinical presentation and therapeutic optionsBriefly describe the function of uridine triphosphate (UTP) in carbohydratemetabolism.What are difference between phenylketoneuria and thalassemia?
- What is hereditary fructose intolerance? Explain briefly.What is the difference between ketogenic and glucogenic amino acids?Amino acid degradation and biosynthesis are related metabolic processes, but they are not identical. Indicate two ways in which they are similar and one in which they are different. Be as specific as you can.
- create or design a concept map explaining in one page using figures, illustrations, and a few descriptions or explanations of the Type 1 glycogen storage disease. The content of your concept map should include the biochemical and molecular basis of the disease with clinical presentation and therapeutic options.What is/are the possible genotype(s) of an individual who is lactose intolerant?Write down the abbreviations (both 1 letter and 3 letter) for the amino acids given below:Tryptophan, Glutamine, Isoleucine, Cysteine, Arginine