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...
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2016-12-01
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Series: | Hematology/Oncology and Stem Cell Therapy |
Online Access: | http://www.sciencedirect.com/science/article/pii/S1658387616300565 |