TY - CHAP M1 - Book, Section TI - Gangliosidosis (GM1) Type I A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Marciniak, Bruno A1 - Dalens, Bernard J. Y1 - 2006 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications AB - Lysosomal storage disease. Affected patients have clinical features resembling those of mucopolysaccharidoses types I and VI but without mucopolysacchariduria. Clinical features include joint stiffness, scoliosis, and skeletal dystrophy. Valvular heart diseases are present, of which aortic insufficiency is the most common. Obstructive sleep apnea is frequent, and 50% of reported cases have mild mental retardation. SN - PB - The McGraw-Hill Companies CY - New York, NY Y2 - 2024/03/29 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=58077506 ER -