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.
Farlex Partner Medical Dictionary © Farlex 2012
Hegg·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.
Medical Dictionary for the Health Professions and Nursing © Farlex 2012
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 anomaly Hegglin syndrome - an energy-dynamic cardiac insufficiency during diabetic coma and other metabolic disorders. Synonym(s):
May-Hegglin syndrome Medical Eponyms © Farlex 2012
References in periodicals archive
Mutations of MYH9, encoding for non-muscle myosin heavy chain A, in May
Hegglin anomaly. Nat Genet 2000;26:106-8.
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