The May-Hegglin Anomaly: Platelet Function, Ultrastructure and Chromosome Studies
Keyword(s):
Abstract A father and son with the May-Hegglin anomaly were studied. Both were asymptomatic, although the father had a mild thrombocytopenia and a probable platelet thromboplastic function defect. Possible mechanisms for the bleeding tendency observed in approximately one-fourth of the persons with this anomaly are discussed. The autosomal dominant mode of inheritance is again demonstrated, and both father and son were found to have normal chromosomes.
1996 ◽
Vol 89
(7)
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pp. 403-408
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2008 ◽
Vol 33
(1)
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pp. 1-4
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2008 ◽
Vol 136
(9-10)
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pp. 542-544
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2012 ◽
Vol 58
(3)
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pp. 22-30
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