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Gahl, W.A., Brantly, M., Kaiser-Kupfer, M.I., Iwata, F., Hazelwood, S., Shotelersuk, V., Duffy, L.F., Kuehl, E.M., Troendle, J. and Bernardini, I. (1998) Genetic Defects and Clinical Characteristics of Patients with a Form of Oculocutaneous Albinism (Hermansky-Pudlak Syndrome). The New England Journal of Medicine, 338, 1258-1264.
http://dx.doi.org/10.1056/NEJM199804303381803

has been cited by the following article:

• TITLE: Anesthetic Management of a Patient with Hermansky-Pudlak Syndrome

  AUTHORS: Kelly Zach, Lopa Misra

  KEYWORDS: Hermanksy-Pudlak, Anesthesia

  JOURNAL NAME: Open Journal of Anesthesiology, Vol.5 No.2, February 26, 2015

  ABSTRACT: Hermansky-Pudlak Syndrome (HPS) is a rare genetic condition characterized by platelet function abnormalities and oculocutaneous albinism. Other systemic manifestations of the disease include pulmonary fibrosis, granulomatous colitis, impaired renal function, and cardiomyopathy. Due to the systemic extent of the disease, HPS has multiple anesthetic concerns and requires a detailed preoperative evaluation and close perioperative monitoring.