Literature DB >> 16169642

Congenital macrothrombocytopenias.

Shinji Kunishima1, Hidehiko Saito.   

Abstract

Congenital macrothrombocytopenias comprise a heterogeneous group of rare disorders, characterized by abnormal giant platelets, thrombocytopenia and bleeding tendency with variable severity. Many of these disorders share common clinical and laboratory features, making accurate diagnosis difficult and patients are often misdiagnosed with and treated for idiopathic thrombocytopenic purpura. Recent progress in the elucidation of underlying defects and further developments of specific diagnostic techniques for several congenital macrothrombocytopenias have renewed our approach to the classification and the diagnosis of the disease. This review summarizes the current knowledge on the clinical and laboratory features of common congenital macrothrombocytopenias and discusses how that knowledge aids in making a proper diagnosis.

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Year:  2005        PMID: 16169642     DOI: 10.1016/j.blre.2005.08.001

Source DB:  PubMed          Journal:  Blood Rev        ISSN: 0268-960X            Impact factor:   8.250


  10 in total

1.  Bernard-Soulier syndrome due to GPIX W127X mutation in Japan is frequently misdiagnosed as idiopathic thrombocytopenic purpura.

Authors:  Shinji Kunishima; Toshiki Yamada; Motohiro Hamaguchi; Hidehiko Saito
Journal:  Int J Hematol       Date:  2006-05       Impact factor: 2.490

Review 2.  Thrombocytopenias: a clinical point of view.

Authors:  Dino Veneri; Massimo Franchini; Federica Randon; Ilaria Nichele; Giovanni Pizzolo; Achille Ambrosetti
Journal:  Blood Transfus       Date:  2009-04       Impact factor: 3.443

3.  ACTN1 mutations cause congenital macrothrombocytopenia.

Authors:  Shinji Kunishima; Yusuke Okuno; Kenichi Yoshida; Yuichi Shiraishi; Masashi Sanada; Hideki Muramatsu; Kenichi Chiba; Hiroko Tanaka; Koji Miyazaki; Michio Sakai; Masatoshi Ohtake; Ryoji Kobayashi; Akihiro Iguchi; Gen Niimi; Makoto Otsu; Yoshiyuki Takahashi; Satoru Miyano; Hidehiko Saito; Seiji Kojima; Seishi Ogawa
Journal:  Am J Hum Genet       Date:  2013-02-21       Impact factor: 11.025

4.  Novel Mutation in Bernard-Soulier Syndrome.

Authors:  Kirstin Sandrock; Ralf Knöfler; Andreas Greinacher; Birgitt Fürll; Sebastian Gerisch; Ulrich Schuler; Siegmund Gehrisch; Anja Busse; Barbara Zieger
Journal:  Transfus Med Hemother       Date:  2010-09-15       Impact factor: 3.747

Review 5.  Inherited Macrothrombocytopenia: Correlating Morphology, Epidemiology, Molecular Pathology and Clinical Features.

Authors:  Kanjaksha Ghosh; Maitreyee Bhattacharya; Ranjini Chowdhury; Kanchan Mishra; Malay Ghosh
Journal:  Indian J Hematol Blood Transfus       Date:  2018-05-05       Impact factor: 0.900

6.  Macrothrombocytopenia in north India: role of automated platelet data in the detection of an under diagnosed entity.

Authors:  Naveen Kakkar; M Joseph John; Amrith Mathew
Journal:  Indian J Hematol Blood Transfus       Date:  2014-04-02       Impact factor: 0.900

Review 7.  Inherited platelet disorders: thrombocytopenias and thrombocytopathies.

Authors:  Giovanna D'Andrea; Massimiliano Chetta; Maurizio Margaglione
Journal:  Blood Transfus       Date:  2009-10       Impact factor: 3.443

8.  ACTN1-related thrombocytopenia: identification of novel families for phenotypic characterization.

Authors:  Roberta Bottega; Caterina Marconi; Michela Faleschini; Gabriele Baj; Claudia Cagioni; Alessandro Pecci; Tommaso Pippucci; Ugo Ramenghi; Simonetta Pardini; Loretta Ngu; Carlo Baronci; Shinji Kunishima; Carlo L Balduini; Marco Seri; Anna Savoia; Patrizia Noris
Journal:  Blood       Date:  2014-10-31       Impact factor: 22.113

9.  The actinin family of actin cross-linking proteins - a genetic perspective.

Authors:  Anita C H Murphy; Paul W Young
Journal:  Cell Biosci       Date:  2015-08-25       Impact factor: 7.133

10.  A GP1BA Variant in a Czech Family with Monoallelic Bernard-Soulier Syndrome.

Authors:  Magdalena Skalníková; Kateřina Staňo Kozubík; Jakub Trizuljak; Zuzana Vrzalová; Lenka Radová; Kamila Réblová; Radka Holbová; Terézia Kurucová; Hana Svozilová; Jiří Štika; Ivona Blaháková; Barbara Dvořáčková; Marie Prudková; Olga Stehlíková; Michal Šmída; Leoš Křen; Petr Smejkal; Šárka Pospíšilová; Michael Doubek
Journal:  Int J Mol Sci       Date:  2022-01-14       Impact factor: 5.923

  10 in total

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