HPS Network Inc. per Usator de Firefox 12175464
ermansky–Pudlak syndrome (HPS) is a rare autosomal recessive disorder which results in oculocutaneous albinism (decreased pigmentation), bleeding problems due to a platelet abnormality (platelet storage pool defect), and storage of an abnormal fat-protein compound (lysosomal accumulation of ceroid lipofuscin). HPS also causes Pulmonar Fibrosis It is considered to affect around 1 in 500,000 people worldwide, with a significantly higher occurrence in Puerto Ricans.
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- Version
- 2.0
- Dimension
- 71,26 KB
- Ultime actualisation
- 6 éve (2019. máj. 13.)
- Categorias associate
- Licentia
- Creative Commons Attribution-NoDerivs 3.0
- Historia de versiones
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