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MBBS DegreeFaculty of Faculty of Medical, Health & Clinical SciencesMedicine & Surgery
BCH 202: Nutrition, Inborn Errors of Metabolism & Metabolic Disorders (200 Level)
Pathobiochemistry of inherited metabolic diseases, glycogen storage disorders, amino acidopathies, porphyrias, obesity, metabolic syndrome, and clinical nutrition.
Course Overview
Pathobiochemistry of inherited metabolic diseases, glycogen storage disorders, amino acidopathies, porphyrias, obesity, metabolic syndrome, and clinical nutrition. Curriculum Structure & Core Modules: • 1. Inborn Errors of Amino Acid Metabolism: Phenylketonuria, Alkaptonuria &...
What You'll Learn
- Detail the enzyme deficiencies, accumulated metabolites, and clinical features of common amino acidopathies.
- Explain the biochemical classification and organ pathology of glycogen and lysosomal storage diseases.
- Trace the heme biosynthetic pathway and differentiate the acute from cutaneous porphyrias.
- Explain the molecular basis of hemoglobin S and C mutations and sickle cell pathophysiology.
- Design evidence-based nutritional strategies for protein-energy malnutrition and metabolic syndrome.
Requirements
- BCH 201 credit
Degree Programme Curriculum Context
This course is a curriculum unit of the Bachelor of Medicine, Bachelor of Surgery (MBBS) degree framework in Nigeria.
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Course Curriculum
Open-access academic curriculum. All foundational lectures available to read free.
8 Chapters
•16 Lecture
•0s
1. Inborn Errors of Amino Acid Metabolism: Phenylketonuria, Alkaptonuria & MSUD: Structural Principles & Pathophysiological Derangements
BCH 202 • 200L • Medical Biochemistry • Chapter 1 • Lecture 1 Inborn Errors of Amino Acid Metabolism: Phenylketonuria, Alkaptonuria & MSUD: Structural Principles, Functional Architecture & Pathophysiological Derangements Curriculum Reference: BCH 202: Nutrition, Inborn Errors of Metabolism & Metabolic Disorders (200 Level) • Metabolic Biochemistry & Bioenergetics &...
2. Inborn Errors of Amino Acid Metabolism: Phenylketonuria, Alkaptonuria & MSUD: Clinical Semiology, Differential Diagnosis & Evidence-Based Management
BCH 202 • 200L • Medical Biochemistry • Chapter 1 • Lecture 2 Inborn Errors of Amino Acid Metabolism: Phenylketonuria, Alkaptonuria & MSUD: Clinical Semiology, Differential Diagnosis & Evidence-Based Bedside Management Curriculum Reference: BCH 202: Nutrition, Inborn Errors of Metabolism & Metabolic Disorders (200 Level) • MDCN Professional MBBS Exam / UK GMC MLA /...
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3. Inborn Errors of Amino Acid Metabolism: Phenylketonuria, Alkaptonuria & MSUD: Formative Clinical Case Assessment
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Instructor
PAMCET Learning Team
Institutional Course Curation · PAMCET
Qualifications:
PAMCET Learning Team — Institutional Course Curation, Digitpen Hub LtdMy Skills:
- Curriculum Curation
- Course Content Review
- Learning Outcome Design
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Free
Course Includes
8 Chapters
16 Lectures
1 week
Skill Level beginner
Taught in English
Lifetime Access
Certification of Completion
Category: University - Medicine & Surgery
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