TY - CHAP M1 - Book, Section TI - Hermansky-Pudlak Syndrome (HPS) A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - Genetically transmitted metabolic disorder causing albinism, visual impairment, platelet pool storage deficiency resulting in bleeding diathesis, and lysosomal accumulation of ceroid lipofuscin resulting in pulmonary fibrosis, inflammatory bowel disease, and renal insufficiency. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164072934 ER -