TY - CHAP M1 - Book, Section TI - Oculocutaneous Albinism Type VIA: Hermansky-Pudlak Syndrome (HPS) A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - Autosomal recessive inherited, tyrosinase-positive oculocutaneous albinism with bleeding diathesis secondary to a platelet storage pool deficiency, and occasionally restrictive lung disease and cardiomyopathy. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164061156 ER -