UREA CYCLE, Part 1, BIOCHEMISTRY LECTURES, PEDIATRICS LECTURES, METABOLIC DISORDERS, INICET, NEETPG

#UREACYCLE, Part 1, #UreaCycleDisorders #BIOCHEMISTRYLECTURES, #PEDIATRICSLECTURES, #METABOLICDISORDERS, #INICET, #NEETPG
The urea cycle (also known as the ornithine cycle) is a cycle of biochemical reactions that produces urea (NH2)2CO from ammonia (NH3). This cycle occurs in ureotelic organisms. The urea cycle converts highly toxic ammonia to urea for excretion.
Primary urea cycle disorders (UCDs) include carbamoyl phosphate synthase (CPS) deficiency, ornithine transcarbamylase (OTC) deficiency, argininosuccinate synthetase deficiency (citrullinemia), argininosuccinate lyase deficiency (argininosuccinic aciduria), and arginase deficiency (argininemia).

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