Related Experiment Video
Updated: Aug 11, 2026

Biochemical Measurement of Neonatal Hypoxia
Published on: August 24, 2011
Ornithine aminotransferase deficiency: diagnostic difficulties in neonatal presentation
M A Cleary1, L Dorland, T J de Koning
1Willink Biochemical Genetics Unit, Royal Manchester Children's Hospital, Pendlebury, Manchester, UK.
Abstract:
We describe two unrelated cases of ornithine aminotransferase (OAT) deficiency with rare neonatal presentation of hyperammonaemia. The diagnosis in the neonatal presentation of OAT deficiency is hampered as hyperornithinaemia is absent. Enzyme and mutation studies confirmed the diagnosis. OAT deficiency should be included in differential diagnosis of neonatal hyperammonaemia.
More Related Videos
06:15Protocol and Guidelines for Point-of-Care Lung Ultrasound in Diagnosing Neonatal Pulmonary Diseases Based on International Expert Consensus
Published on: March 6, 2019
09:31Hemodynamic Precision in the Neonatal Intensive Care Unit using Targeted Neonatal Echocardiography
Published on: January 27, 2023
Related Concept Videos
Urea Cycle
Overview of Protein Metabolism
Amino acids play various roles in the body once they are absorbed into cells. They are restructured...