Chhaparwal, YogeshKumar, MathangiChhaparwal, Shubha2020-11-182020-11-182020-07Chhaparwal Yogesh, Kumar Mathangi, Chhaparwal Shubha. Hermansky Pudlak Syndrome Type 2:A Rare Case Report.. Journal of Krishna Institute of Medical Sciences University. 2020 Jul; 9(3): 97-1012231-4261http://imsear.searo.who.int/handle/123456789/215672Hermansky-Pudlak Syndrome (HPS) is a rareautosomal recessive disorder characterized byOculocutaneous Albinism (OCA), platelet disorder,and ceroid accumulation. It is common in North WestPuerto Rico region, and the incidence reported is1/500000. It is a rare genetic disorder with plateletdysfunction resulting in bleeding diathesis. Here wereport one such rare case of HPS type 2 in a 7-year-oldboy with difficulty in chewing.oculocutaneous albinismHermansky Pudlak syndromeplatelet disorderJournal ArticleIndiaDepartment of Oral Medicine and Radiology, Manipal College of Dental Sciences, Manipal, Manipal Academy of Higher Education, Manipal 576104 (Karnataka), IndiaDepartment of Conservative Dentistry and Endodontics, Manipal College of Dental Sciences, Manipal, Manipal Academy of Higher Education, Manipal 576104 (Karnataka), India