| Literature DB >> 27514596 |
Souheil El-Chemaly1, Lisa R Young2.
Abstract
Hermansky-Pudlak syndrome (HPS) is an autosomal recessive disorder that is associated with oculocutaneous albinism, bleeding diatheses, granulomatous colitis, and highly penetrant pulmonary fibrosis in some subtypes, including HPS-1, HPS-2, and HPS-4. HPS pulmonary fibrosis shows many of the clinical, radiologic, and histologic features found in idiopathic pulmonary fibrosis, but occurs at a younger age. Despite knowledge of the underlying genetic defects, there are currently no definitive therapeutic or preventive approaches for HPS pulmonary fibrosis other than lung transplant.Entities:
Keywords: Adaptor protein 3; Albinism; Biogenesis of lysosome-related organelle complex; Hermansky-Pudlak syndrome; Interstitial lung disease; Pulmonary fibrosis
Mesh:
Year: 2016 PMID: 27514596 PMCID: PMC4987498 DOI: 10.1016/j.ccm.2016.04.012
Source DB: PubMed Journal: Clin Chest Med ISSN: 0272-5231 Impact factor: 2.878