Lung Cancer© Volume 4 - Issue 1

Andrew Hague*

• Professor Andrew Hague, President of Cell Sonic Limited, UK

Received: December 14, 2021;  Published: January 06, 2021

Corresponding author: Andrew Hague, Professor Andrew Hague, President of Cell Sonic Limited, UK

DOI: 10.32474/GJAPM.2020.04.000177

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Abstract

Citrullinemia is an autosomal recessive genetic condition that falls under the spectrum of urea cycle disorders. The defective genes reduce the activity of enzymes needed to process nitrogen effectively. Two types exist: type I (neonatal onset) occurs when the defective arginosuccinate synthase enzyme fails to complete the third step of the urea cycle by converting citrulline and aspartate to L-argininosuccinate. Type II (adult onset) develops with the production of malfunctioning citrine proteins, which serve to transport molecules used in the metabolism of simple sugars, the assembly of protein, and the urea cycle

Abstract| The Lady Patient| Protocol| The Immune System| Conclusion|