Literature DB >> 7330822

Glanzmann's thrombasthenia. A review and report of 42 cases from South India.

U Khanduri, R Pulimood, A Sudarsanam, R H Carman, M Jadhav, S Pereira.   

Abstract

In the 14 year period from June, 1966 to June, 1980, 42 cases of Glanzmann's thrombasthenia have been diagnosed, all fulfilling the criteria of prolonged bleeding time, with normal venous platelet count, defective clot retraction and decreased platelet aggregation, associated with a lifelong bleeding tendency. Few cases have been reported from India though it is the fourth most common congenital bleeding disorder among the patients seen at the Christian Medical College Hospital, Vellore. The large number of such cases found in South India as compared with reports from other parts of the world may be due to the high degree of consanguinity which is part of the accepted culture in this area. Reliable diagnosis of this condition is possible with fairly simple laboratory procedures.

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Year:  1981        PMID: 7330822

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN: 0340-6245            Impact factor:   5.249


  9 in total

1.  Haematology research in India: past, present and future.

Authors:  Kanjaksha Ghosh
Journal:  Indian J Hematol Blood Transfus       Date:  2011-05-08       Impact factor: 0.900

2.  Leukocyte Adhesion Deficiency-I: Clinical and Molecular Characterization in an Indian Population.

Authors:  Prashant Deshpande; Kotteeswari Kathirvel; Ansu Abu Alex; Anu Korula; Biju George; R V Shaji; Vikram Mathews
Journal:  Indian J Pediatr       Date:  2016-02-29       Impact factor: 1.967

Review 3.  Glanzmann's thrombasthenia.

Authors:  M S Tullu; P S Dixit; S B Nair; J R Kamat; R K Vaswani; S D Shetty; A R Pawar
Journal:  Indian J Pediatr       Date:  2001-06       Impact factor: 1.967

4.  Specifications of the variant curation guidelines for ITGA2B/ITGB3: ClinGen Platelet Disorder Variant Curation Panel.

Authors:  Justyne E Ross; Bing M Zhang; Kristy Lee; Shruthi Mohan; Brian R Branchford; Paul Bray; Stefanie N Dugan; Kathleen Freson; Paula G Heller; Walter H A Kahr; Michele P Lambert; Lori Luchtman-Jones; Minjie Luo; Juliana Perez Botero; Matthew T Rondina; Gabriella Ryan; Sarah Westbury; Wolfgang Bergmeier; Jorge Di Paola
Journal:  Blood Adv       Date:  2021-01-26

5.  A 13-bp deletion in alpha(IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia.

Authors:  N Rosenberg; H Hauschner; H Peretz; R Mor-Cohen; M Landau; B Shenkman; G Kenet; B S Coller; A A Awidi; U Seligsohn
Journal:  J Thromb Haemost       Date:  2005-12       Impact factor: 5.824

Review 6.  Glanzmann's thrombasthenia: report of a case and review of the literature.

Authors:  Christopher Sebastiano; Michael Bromberg; Karen Breen; Matthew T Hurford
Journal:  Int J Clin Exp Pathol       Date:  2010-04-25

7.  αIIbβ3 variants defined by next-generation sequencing: predicting variants likely to cause Glanzmann thrombasthenia.

Authors:  Lorena Buitrago; Augusto Rendon; Yupu Liang; Ilenia Simeoni; Ana Negri; Marta Filizola; Willem H Ouwehand; Barry S Coller
Journal:  Proc Natl Acad Sci U S A       Date:  2015-03-31       Impact factor: 11.205

8.  Bleeding disorders in the tribe: result of consanguineous in breeding.

Authors:  Munira Borhany; Zaen Pahore; Zeeshan Ul Qadr; Muhammad Rehan; Arshi Naz; Asif Khan; Saqib Ansari; Tasneem Farzana; Muhammad Nadeem; Syed Amir Raza; Tahir Shamsi
Journal:  Orphanet J Rare Dis       Date:  2010-09-07       Impact factor: 4.123

9.  GLANZMANN's THROMBASTHENIA-SPECTRUM OF CLINICAL PRESENTATION ON SAUDI PATIENTS IN THE EASTERN PROVINCE.

Authors:  S K Ai-Barghouthi; A Ai-Othman; A Lardhi
Journal:  J Family Community Med       Date:  1997-01
  9 in total

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