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Two cases of Glanzmann's thrombasthenia in brother.

Journal of the Korean Pediatric Society 1989;32(11):1574-1580.
Published online November 30, 1989.
Two cases of Glanzmann's thrombasthenia in brother.
Won Mo Yang1, Hyung Kook Ham1, Mee Kyung Namgoong1, Baek Keun Lim1, Hong Sup Yoon2, Kab Joon Yoon2
1Department of Pediatrics, Wonju College of Medicine, Yonsei University Wonju, Korea
2Department of Clinical Pathology, Wonju College of Medicine, Yonsei University Wonju, Korea
형제에서 발생된 혈소판무력증 2례
양원모1, 함형국1, 남궁미경1, 임백근1, 윤홍섭2, 윤갑준2
1연세대학교 원주의과대학 소아과학교실
2연세대학교 원주의과대학 임상병리과학교실
Received: 17 May 1989   • Accepted: 9 August 1989
Abstract
Glanzmann’s thrombasthenia is rare congenital bleeding disorder of autosomal recessive trait. We experienced two cases of Glanzmann’s thrombasthenia in brother. The mother and elder brother had no history of bleeding tendency. But 10 year-old and 7 year-old younger brothers had frequent epistaxis, gum bleeding and easy bruisability. On platelet aggregation test, mother and elder brother appeared normal responses, but the younger brothers appeared no responses to ADP, epinephrine and collagen, with normal response to ristocetin. We report two cases of Glanzmann’s thrombasthenia in brother with review of literatures briefly.
Key Words: Glanzmann’s thrombasthenia, Platelet aggregation test


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