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Original Article
A case of thrombasthenia.
Yong Bae Suh, Eun Kyoung Sohn, Yong Mook Choi, Chang Il Ahn
Clin Exp Pediatr. 1991;34(2):287-291.   Published online February 28, 1991
Glanzmann’s thrombasthenia is a congenital disorder of platelet function with missing or abnormal platelet plasma membrane glycoprotein Ilb/IIIa which function as receptors for fibrinogen and other high-molecular-weight adhesive proteins which are important for platelet aggregation. We have experienced a case of thrombasthenia in a 12 month old male whose chief complaints were easy bruising and frequent epistaxis. The beeding time was prolonged in the...
Two cases of Glanzmann's thrombasthenia in brother.
Won Mo Yang, Hyung Kook Ham, Mee Kyung Namgoong, Baek Keun Lim, Hong Sup Yoon, Kab Joon Yoon
Clin Exp Pediatr. 1989;32(11):1574-1580.   Published online November 30, 1989
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...
A Case of Glanzmann's Thrombathenia.
Saeng Gu Cho, Won Ho Kang, Young Youn Choi, Tai Ju Hwang, Dong Wook Ryang, Joo Young Yoo
Clin Exp Pediatr. 1986;29(6):668-673.   Published online June 30, 1986
The authors experienced a 6-year-old female patient with Glanzmann’s Thrombathenia and cerebral palsy. She was admitted with epistaxis, gingival bleeding and easy bruisability. Platelets of patients showed complete absence of aggreration in response to ADP, collagen, and epinephrine but only first aggregation to ristocetin. After platelet aggregation test, bone marrow aspiration, and electron micrographic examination, she was proved as...
Case Report
A case of Thrombasthenia.
Sung Sook Cho, Kye Tai Kim, Don Hee Ahn, Keun Chan Sohn
Clin Exp Pediatr. 1981;24(1):88-93.   Published online January 15, 1981
A 6 year 6month-old boy was admitted with complains of severe spontaneou epistaxis and easy brusability. He was one of five siblings, and two of them died of recurred severe epistaxis at their age of six years. There was no history of bleeding tendency to his antecedents and parents, whose marriage was unrelated. Platelet count and partial thromboplastin time were...