TY - CHAP M1 - Book, Section TI - Lysinuric Protein Intolerance A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - It is an autosomal recessive disease characterized by defective transport of the dibasic amino acids. Clinically, it is characterized by failure to thrive, poor growth during childhood, hepatomegaly, splenomegaly, lung involvement, sparse hair, and muscle hypotonia. Patients affected present a normal development to moderate mental retardation. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164077493 ER -