Storage pool disease Other manifestations- epistaxis ,menorrhagia, easy bruising, autosomal recessive. Hermansky-Pudlak  Syndrome occlulocutaneous  albinism, platelet function abnormality, congenital neutropenia, pulmonary fibrosis and granulomatous colitis Quebec platelet disorder bleeding, autosomal dominant (unlikely) Glanzmann’s thrombasthenia Was described in 1918-has impaired aggregation of platelets to collagen, ADP or epinephrine-causes menorrhagia, petechial and purpura. It is autosomal dominant.

Table 2: Could our patients with endomyocardial fibrosis have any of these ?