TY  - CHAP
M1  - Book, Section
TI  - Hermansky-Pudlak Syndrome (HPS)
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
Y1  - 2019
N1  - 
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  - 2024/04/23
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164072934
ER  -