TY - CHAP M1 - Book, Section TI - D-Glyceric Acidemia A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - It is part of a group of inborn error of metabolism resulting in D-glyceric academia. The clinical features include a progressive encephalopathy, severe mental/psychomotor retardation, seizures, microcephaly, hypotonia, failure to thrive, severe metabolic acidosis, and early death in the full expressed disorder, whereas those affected with the mild phenotype have light speech delay or even normal development. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/11/11 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164067862 ER -