## Abstract Hermansky–Pudlak syndrome (HPS) is a rare autosomal recessive disorder characterized by oculocutaneous albinism and a platelet storage pool deficiency. Some patients also develop fatal pulmonary fibrosis and some have granulomatous colitis. Six human genes __HPS1__, __ADB3A__, __HPS3__,
✦ LIBER ✦
A case of deep vein thrombosis in patient with Hermansky–Pudlak syndrome
✍ Scribed by Randi Katz; Dana Shani
- Publisher
- Springer
- Year
- 2005
- Tongue
- English
- Weight
- 42 KB
- Volume
- 84
- Category
- Article
- ISSN
- 0939-5555
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