TY - CHAP M1 - Book, Section TI - Ornithine Delta-Aminotransferase Deficiency A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - Rare genetic disorder affecting mitochondrial metabolism of ornithine. It is characterized by the presence of gyrate atrophy of the retina leading to night blindness that begins in late childhood, accompanied by sharply demarcated circular areas of chorioretinal atrophy. Early degenerative, atrophic brain changes and abnormal EEG are features of gyrate atrophy, in addition to the well-characterized eye and muscle manifestations. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164080704 ER -