Literature DB >> 453097

Alport's syndrome associated with macrothrombopathic thrombocytopenia.

N M Clare, M M Montiel, M D Lifschitz, G A Bannayan.   

Abstract

The combined occurrence of hereditary nephritis with nerve deafness (Alport's syndrome) and macrothrombocytopathic thrombocytopenia is very rare. The authors have had the opportunity to study such a case in a 20-year-old man who had been followed since birth. The clinical history, renal biopsy, platelet studies, and autopsy findings are presented. The renal pathologic findings are well defined; however, the hemostatic abnormalities and the hearing loss are not well characterized. In this paper, an attept is made to clarify the diverse platelet functional and morphologic abnormalties.

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Year:  1979        PMID: 453097     DOI: 10.1093/ajcp/72.1.111

Source DB:  PubMed          Journal:  Am J Clin Pathol        ISSN: 0002-9173            Impact factor:   2.493


  7 in total

1.  Glomerular pathology in autosomal dominant MYH9 spectrum disorders: what are the clues telling us about disease mechanism?

Authors:  Jeffrey B Kopp
Journal:  Kidney Int       Date:  2010-07       Impact factor: 10.612

2.  Mapping of Alport syndrome to the long arm of the X chromosome.

Authors:  C L Atkin; S J Hasstedt; L Menlove; L Cannon; N Kirschner; C Schwartz; K Nguyen; M Skolnick
Journal:  Am J Hum Genet       Date:  1988-02       Impact factor: 11.025

3.  Genetic linkage of autosomal-dominant Alport syndrome with leukocyte inclusions and macrothrombocytopenia (Fechtner syndrome) to chromosome 22q11-13.

Authors:  A Toren; N Amariglio; G Rozenfeld-Granot; A J Simon; F Brok-Simoni; E Pras; G Rechavi
Journal:  Am J Hum Genet       Date:  1999-12       Impact factor: 11.025

Review 4.  Epstein's syndrome: case report and survey of the literature.

Authors:  G R Standen; J Saunders; J Michael; A L Bloom
Journal:  Postgrad Med J       Date:  1987-07       Impact factor: 2.401

5.  Hereditary nephritis, platelet disorders and deafness-Epstein's syndrome.

Authors:  S Túri; J Kóbor; A Erdös; T Bodrogi; I Virág; J Ormos
Journal:  Pediatr Nephrol       Date:  1992-01       Impact factor: 3.714

6.  Genetic heterogeneity among kindreds with Alport syndrome.

Authors:  S J Hasstedt; C L Atkin; A C San Juan
Journal:  Am J Hum Genet       Date:  1986-06       Impact factor: 11.025

7.  MYH9-related disorders display heterogeneous kidney involvement and outcome.

Authors:  Nahid Tabibzadeh; Dominique Fleury; Delphine Labatut; Frank Bridoux; Arnaud Lionet; Noémie Jourde-Chiche; François Vrtovsnik; Nicole Schlegel; Philippe Vanhille
Journal:  Clin Kidney J       Date:  2018-12-17
  7 in total

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