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:: Volume 7, Issue 2 (Autumn & Winter 2005) ::
J Gorgan Univ Med Sci 2005, 7(2): 71-73 Back to browse issues page
TAR syndrome (Case Report)
NB.Mirbehbahani (MD) * 1, M.Fooladinejhad (MD)
Abstract:   (19212 Views)
Diagnsis of TAR syndrome usually are made at birth because of the characteristic physical appearace combined with thocmbocytopenia. The Two essential features of TAR syndrome are hypomegakaryocytic thrombocytopenia and bilateral radial aplasia. The rest of the phenotype varies widely and can manifest with abnormalities involving skeletal, skin, gasterointestinal and cardiac systems. Considering to limited cases of syndrome and variability of phenotypic abnormalities exess two essential features, all cases of this syndrome are reportable. We reported a patient with TAR syndrome with any related malformations.
Keywords: TAR syndrome, Thrombocytopenia, Radius
Full-Text [PDF 193 kb] [English Abstract]   (26178 Downloads)    
Type of Study: Case Report | Subject: General
* Corresponding Author Address: Department of Pediatrics&Oncology Gorgan University of Medical Sciences. n.mirbehbahani@gmail.com


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NB.Mirbehbahani (MD), M.Fooladinejhad (MD). TAR syndrome (Case Report). J Gorgan Univ Med Sci 2005; 7 (2) :71-73
URL: http://goums.ac.ir/journal/article-1-41-en.html


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Volume 7, Issue 2 (Autumn & Winter 2005) Back to browse issues page
مجله دانشگاه علوم پزشکی گرگان Journal of Gorgan University of Medical Sciences
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This work is licensed under a Creative Commons — Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)