TAR SYNDROME (CASE REPORT)

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MIRBEHBAHANI N.B.; FOULADINEZHAD M.

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Journal Paper

Paper Information

Journal: Journal of Gorgan University of Medical Sciences Year:2005 | Volume:7 | Issue:2 (16) Page(s): 71-73

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Information Journal Paper

Title

TAR SYNDROME (CASE REPORT)

Author(s)

MIRBEHBAHANI N.B. | FOULADINEZHAD M. | Issue Writer Certificate

Keywords

TAR SYNDROMEQ4

THROMBOCYTOPENIAQ3

RADIUSQ3

Abstract

Diagnosis of TAR SYNDROME usually is made at birth because of the characteristic physical appearance combined with THROMBOCYTOPENIA. 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, gastrointestinal 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.

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APA: Copy

MIRBEHBAHANI, N.B., & FOULADINEZHAD, M.. (2005). TAR SYNDROME (CASE REPORT). JOURNAL OF GORGAN UNIVERSITY OF MEDICAL SCIENCES, 7(2 (16)), 71-73. SID. https://sid.ir/paper/79545/en

Vancouver: Copy

MIRBEHBAHANI N.B., FOULADINEZHAD M.. TAR SYNDROME (CASE REPORT). JOURNAL OF GORGAN UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2005;7(2 (16)):71-73. Available from: https://sid.ir/paper/79545/en

IEEE: Copy

N.B. MIRBEHBAHANI, and M. FOULADINEZHAD, “TAR SYNDROME (CASE REPORT),” JOURNAL OF GORGAN UNIVERSITY OF MEDICAL SCIENCES, vol. 7, no. 2 (16), pp. 71–73, 2005, [Online]. Available: https://sid.ir/paper/79545/en

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