MYH9-related disorder, a probable May–Hegglin anomaly case series: A tertiary care experience

Objective/background: May–Hegglin anomaly (MHA) is a rare familial bleeding disorder characterized by a triad of thrombocytopenia, giant platelets, and Döhle-like inclusion bodies within the leukocytes. The clinical spectrum as well as the pathophysiology of this entity is not well defined. The obje...

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Bibliographic Details
Main Authors: Vandana Kamath, Kiruthiga Kala Gnanasekaran, Joy Mammen
Format: Article
Language:English
Published: Elsevier 2016-12-01
Series:Hematology/Oncology and Stem Cell Therapy
Online Access:http://www.sciencedirect.com/science/article/pii/S1658387616300565