CHAPTER ONE
1.0Â Â Â Introduction
1.1Â Â Â Â Inborn errors of metabolism
1.2 Â Biochemical basis for hereditary metabolic diseases
CHAPTER TWO
2.0Â Â Â Â Clinical manifestations and diagnosis of inborn error of Metabolism
2.1Â Â Â Â Clinical manifestation in neonatal period and childhood
2.1.1Â Acute metabolic encephalopathy
2.1.1.1 Hyperammonemia
2.1.1.2 Metabolic acidosis
2.1.1.3 Hypoglycemia
2.1.1.4 Jaundice and liver dysfunction
2.2Â Â Â Â Clinical manifestation in adult
2.3Â Â Â Â Diagnosis
CHAPTER THREE
3.0Â Â Â Treatment of inborn errors of metabolism
CHAPTER FOUR
4.0Â Â Â Â Conclusion and Recommendation
4.1Â Â Â Â Conclusion
4.2Â Â Â Â Recommendation
References
LIST OF FIGURES
Figure 1 – An integrated view of metabolic pathway
Figure 2 – Theoretical consequences of enzyme deficiency
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