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May-Hegglin Anomaly Diagnosed by Genetic Study in a Newborn Infant / 대한주산의학회잡지
Article in Ko | WPRIM | ID: wpr-226169
Responsible library: WPRO
ABSTRACT
May-Hegglin anomaly is an autosomal dominant platelet disorder characterized by giant platelets, thrombocytopenia, and Dohle-like cytoplasmic inclusion bodies in granulocyte. Usually, diagnosis was delayed because they do not have life-threatening bleeding. We experienced a case of May-Hegglin anomaly, which was diagnosed with genetic study at neonate. A 3 days old female has bilateral cephalhematoma at birth after a Caesarean section delivery. Thrombocytopenia with inclusion bodies in granulocyte was observed at peripheral blood cell morphology. Her mother had thrombocytopenia at pregnancy and was diagnosed May-Hegglin anomaly through MYH9 mutation gene study. Accordingly, infant had genetic study and found same gene mutation with mother. Based on the family history, we can diagnose May-Hegglin anomaly in a newborn infant who has cephalhematoma and thrombocytopenia by genetic study.
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Full text: 1 Index: WPRIM Main subject: Thrombocytopenia / Blood Cells / Blood Platelets / Inclusion Bodies / Cesarean Section / Parturition / Granulocytes / Hemorrhage / Mothers Type of study: Diagnostic_studies Limits: Female / Humans / Infant / Newborn / Pregnancy Language: Ko Journal: Korean Journal of Perinatology Year: 2012 Type: Article
Full text: 1 Index: WPRIM Main subject: Thrombocytopenia / Blood Cells / Blood Platelets / Inclusion Bodies / Cesarean Section / Parturition / Granulocytes / Hemorrhage / Mothers Type of study: Diagnostic_studies Limits: Female / Humans / Infant / Newborn / Pregnancy Language: Ko Journal: Korean Journal of Perinatology Year: 2012 Type: Article