Clinical Biochemical Genetics

Biochemical Genetics involves testing and determining inherited metabolic disease, monitoring of treating, and distinguishing heterozygous carriers from non-carriers by metabolite and enzymatic analysis of physiological fluids and tissues in patients. Hereditary metabolic disorders are tested by extremely specialized and fragmented activity, and mostly by research-oriented scientists.

  • Inborn errors of metabolism
  • Malabsorption
  • Malnutrition disorders

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