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May–Hegglin anomaly
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May–Hegglin anomaly : ウィキペディア英語版
May–Hegglin anomaly

May–Hegglin anomaly (MHA), also known as Dohle leukocyte inclusions with giant platelets and macrothrombocytopenia with leukocyte inclusions, is a rare genetic disorder of the blood platelets that causes them to be abnormally large.
==History==
MHA is named for German physician Richard May (January 7, 1863 – 1936) and Swiss physician Robert Hegglin.〔R. May. Leukocyteneinschlüsse. Kasuistische Mitteilung. Deutsches Archiv für klinische Medizin, Leipzig, 1909, 96: 1-6.〕〔R. Hegglin. Über eine neue Form einer konstitutionellen Leukozytenanomalie, kombiniert mit Throbopathie. Schweizerische medizinische Wochenschrift, Basel, 1945, 75: 91-92.〕 The disorder was first described by Richard May in 1909 and was subsequently described by Robert Hegglin in 1945.

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