| 单词 |
hegglin anomaly |
| 释义 |
Hegglin anomaly Hegg·lin a·nom·a·ly (heg'lin), a disorder in which neutrophils and eosinophils contain basophilic structures known as Döhle or Amato bodies and in which there is faulty maturation of platelets, with thrombocytopenia; autosomal dominant inheritance. Synonym(s): May-Hegglin anomalyHegg·lin a·nom·a·ly (heg'lin ă-nom'ă-lē) A disorder in which neutrophils and eosinophils contain basophilic structures known as Döhle or Amato bodies and in which there is faulty maturation of platelets, with thrombocytopenia; autosomal dominant inheritance. Hegglin, Robert M.P., Swiss internist, 1907-1970. Hegglin anomaly - a disorder in which neutrophils and eosinophils contain Döhle bodies and in which there is faulty maturation of platelets, with thrombocytopenia. Synonym(s): May-Hegglin anomalyHegglin syndrome - an energy-dynamic cardiac insufficiency during diabetic coma and other metabolic disorders. Synonym(s): May-Hegglin syndromeMay-Hegglin anomaly - Synonym(s): Hegglin anomalyMay-Hegglin syndrome - Synonym(s): Hegglin syndrome |
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