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
Related Conference of Clinical Biochemical Genetics
November 26-27, 2024
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Clinical Biochemical Genetics Conference Speakers
Recommended Sessions
- Advanced Treatments of Diabetes and Metabolic Syndrome
- Cardio-Metabolic Diseases
- Cholesterol Metabolism
- Clinical Biochemical Genetics
- COVID-19 and Diabetes
- Diabetes and Oral Health
- Diabetes Mellitus and Metabolic Disorders
- Diabetic Education and Healthcare Professionals
- Diabetic Eye Complications
- Diabetic Heart Diseases and Management
- Endocrine Oncology
- Endocrinology
- Gestational Diabetes
- Inherited or Inborn Metabolic Disorders
- Lipid Metabolism
- Medical Devices in Diabetes Treatment
- Medicinal Plants for Metabolic Disorders
- Metabolic Brain Diseases
- Metabolic Liver Diseases
- Metabolic Syndrome
- Metabolism and Metabolic Disorders
- Obesity and Metabolic Disorders
- Pancreas Disorder and Islet Transplantation
- Pediatric Metabolic Disorders
- Prevention & Management of Metabolic Disease
- Reproductive Endocrinology and Infertility
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