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  • Glanzmann thrombasthenia
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  • thrombasthenia
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  • Glanzmann thrombasthenia
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  • hereditary thrombasthenia
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  • hereditary thrombasthenia
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  • thrombasthenia
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  • hereditary thrombasthenia
    À¯Àü¼º Ç÷¼ÒÆÇ ¹«·ÂÁõ(?Ì´ËÛ̬ËÎËçÌ¡).
  • hereditary thrombasthenia
    À¯Àü¼º Ç÷¼ÒÆÇ ¹«·ÂÁõ(¡­úìá³÷ùÙíæ³ñø).
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GT gait training; galactosyl transferase; gastrostomy; generation time; genetic therapy; gingiva treatm...
GTA gene transfer agent; Glanzmann thrombasthenia; glycerol teichoic acid
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thrombasthenia <haematology> Condition in which there is defective platelet aggregation, though adherence is normal.
See: Glanzmann's thrombasthenia.
(18 Nov 1997)
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Glanzmann's thrombasthenia <haematology> A form of congenital platelet functional defect that result in prolongation of the bleeding time. Characteristics include mucosal and post-operative bleeding that may be severe.
(17 Dec 1997)
hereditary haemorrhagic thrombasthenia <haematology> A form of congenital platelet functional defect that result in prolongation of the bleeding time. Characteristics include mucosal and post-operative bleeding that may be severe.
(17 Dec 1997)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 1 ÆäÀÌÁö: 1
  • Thrombasthenia - »õâ A congenital bleeding disorder with prolonged bleeding time, absence of aggregation of platelets in response to most agents, especially ADP, and impaired or absent clot retraction. Platelet membranes are deficient in or have a defect in the glycoprotein IIb-IIIa complex (PLATELET GLYCOPROTEIN GPIIB-IIIA COMPLEX).
    Synonyms : Thrombasthenia, Glanzmann, Thrombasthenias
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thrombasthenia 1. decreased platelet function; called also thromboasthenia.  2. Glanzmann t.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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thrombasthenia a rare autosomal recessive disease in which the platelets do not produce clots in the normal way and hemorrhage results
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