May-Hegglin anomaly: A case of vaginal delivery when both mother and fetus are affected

A. C. Urato, John Repke

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

May-Hegglin anomaly is a rare, autosomal dominant disorder characterized by thrombocytopenia and a variable bleeding tendency. In almost all the case reports in the recent literature, platelet transfusion and cesarean section were performed to avoid maternal and neonatal bleeding. We present a case of a woman with May-Hegglin anomaly who had no history of a bleeding tendency. She had a vaginal delivery and a platelet count of 16,000/mm3; the neonate's platelet count was 35,000/mm3. There were no complications. We advocate a reappraisal of basing platelet transfusion and mode of delivery on the platelet count in patients with May-Hegglin anomaly.

Original languageEnglish (US)
Pages (from-to)260-261
Number of pages2
JournalAmerican Journal of Obstetrics and Gynecology
Volume179
Issue number1
DOIs
StatePublished - Jan 1 1998

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Platelet Count
Platelet Transfusion
Fetus
Mothers
Hemorrhage
Cesarean Section
Thrombocytopenia
Newborn Infant
MYH9-Related Disorders

All Science Journal Classification (ASJC) codes

  • Obstetrics and Gynecology

Cite this

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May-Hegglin anomaly : A case of vaginal delivery when both mother and fetus are affected. / Urato, A. C.; Repke, John.

In: American Journal of Obstetrics and Gynecology, Vol. 179, No. 1, 01.01.1998, p. 260-261.

Research output: Contribution to journalArticle

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