TY - CHAP M1 - Book, Section TI - Prolidase Deficiency A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - A rare congenital disorder of the small peptides metabolism (imidazoles dipeptides). It is characterized by mild to severe skin lesions (mostly the face, palms, lower legs, and soles), cognitive impairment, splenomegaly, recurrent infections involving mainly the respiratory system, and iminodipeptiduria. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164082467 ER -