TY - CHAP M1 - Book, Section TI - Molybdenum Cofactor Deficiency A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas Y1 - 2019 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - It is an extremely rare severe progressive neurodegenerative and neurometabolic disease, characterized by convulsions, severe mental and motor retardation resistant to the treatment. Other features include spastic tetraparesis, brain atrophy, abnormal muscle tone, myoclonic spasms, dislocated lenses, and xanthine urinary stones. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164079110 ER -