| Literature DB >> 30317187 |
Nassreen Abdullah1,2, Niall F Davis1,2, John Quinn3, Ponnusamy Mohan1,2.
Abstract
Hermansky-Pudlak syndrome (HPS) is a rare genetic disorder characterised by oculocutaneous albinism, bleeding diathesis and end-stage renal disease (ESRD), due to interstitial deposition of ceroid lipofuscin. Renal transplantation is potentially a definitive treatment option for patients with ESRD due to HPS. Herein, we describe the case of a 55-year-old male patient with HPS that successfully underwent a living donor kidney transplant. We also emphasise the importance of multidisciplinary input during the preoperative, perioperative and postoperative phases in this high-risk clinical scenario. © BMJ Publishing Group Limited 2018. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: haematology (incl blood transfusion); renal transplantation; transplantation; urological surgery
Mesh:
Year: 2018 PMID: 30317187 PMCID: PMC6194378 DOI: 10.1136/bcr-2017-223376
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X