TY - CHAP M1 - Book, Section TI - Myoadenylate Deaminase Deficiency A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Marciniak, Bruno A1 - Dalens, Bernard J. PY - 2006 T2 - Syndromes: Rapid Recognition and Perioperative Implications AB - Inherited or secondarily acquired disorder of muscle purine nucleotide metabolism. The clinical manifestations include exercise-induced myopathy, postexertional muscle weakness or cramping, prolonged fatigue after exertion, and limping infant caused by benign congenital hypotonia. Generalized muscle pair is often manifested. SN - PB - The McGraw-Hill Companies CY - New York, NY Y2 - 2024/03/29 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=58077050 ER -