<p> </p><p>

Chapter ONE

</p><p>1.0 &nbsp; Introduction</p><p>1.1 &nbsp; &nbsp; Inborn errors of metabolism</p><p>1.2 &nbsp; Biochemical basis for hereditary metabolic diseases</p><p>

Chapter TWO

</p><p>2.0 &nbsp; &nbsp; Clinical manifestations and diagnosis of inborn error of Metabolism</p><p>2.1 &nbsp; &nbsp; Clinical manifestation in neonatal period and childhood</p><p>2.1.1 Acute metabolic encephalopathy</p><p>2.1.1.1 Hyperammonemia</p><p>2.1.1.2 Metabolic acidosis</p><p>2.1.1.3 Hypoglycemia</p><p>2.1.1.4 Jaundice and liver dysfunction</p><p>2.2 &nbsp; &nbsp; Clinical manifestation in adult</p><p>2.3 &nbsp; &nbsp; Diagnosis</p><p>

Chapter THREE

</p><p>3.0 &nbsp; Treatment of inborn errors of metabolism</p><p>

Chapter FOUR

</p><p>4.0 &nbsp; &nbsp; Conclusion and Recommendation</p><p>4.1 &nbsp; &nbsp; Conclusion</p><p>4.2 &nbsp; &nbsp; Recommendation</p><p>References</p><p>LIST OF FIGURES</p><p>Figure 1 – An integrated view of metabolic pathway</p><p>Figure 2 – Theoretical consequences of enzyme deficiency</p> <br><p></p>