Literature DB >> 945691

Thrombocytopenia, macrothrombocytopathia, nephritis and deafness.

J Bernheim, M Dechavanne, P A Bryon, M Lagarde, S Colon, N Pozet, J Traeger.   

Abstract

The association of thrombocytopenia, macrothrombocytopathia, nephritis and deafness is rare. Reported here is a new case of this triple association. The clinical course, the nephropathologic findings and the bilateral neurologic hearing loss were similar to those already reported, with a slowly progressive impairment of renal function accompanied by a persistent proteinuria. The platelet diameters were increased. These macroplatelets contained granules of normal structure but with an irregular distribution in the cytoplasm. In other areas the cytoplasm was rich in surface connected system. The survival of these platelets and their contraction were normal. Their aggregation and excretion in response to collagen, adenosine diphosphate and thrombin, and the values of platelet factor 3 activity were all decreased. The degranulation defect, also present, was observed in the absence of a decrease in intracellular cyclic adenosine 5'-monophosphate (AMP) suggesting a relationship between these two findings.

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Year:  1976        PMID: 945691     DOI: 10.1016/0002-9343(76)90058-9

Source DB:  PubMed          Journal:  Am J Med        ISSN: 0002-9343            Impact factor:   4.965


  6 in total

1.  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

2.  Long term prognosis of recurrent haematuria.

Authors:  P F Miller; N I Speirs; S R Aparicio; M Lendon; J M Savage; R J Postlethwaite; J T Brocklebank; I B Houston; S R Meadow
Journal:  Arch Dis Child       Date:  1985-05       Impact factor: 3.791

Review 3.  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

4.  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

Review 5.  Variants of Alport's syndrome.

Authors:  J P Grünfeld; G Grateau; L H Noel; R Charbonneau; M C Gubler; C O Savage; C M Lockwood
Journal:  Pediatr Nephrol       Date:  1987-07       Impact factor: 3.714

6.  An unusual cause of renal failure; Epstein syndrome.

Authors:  Manish R Balwani; Divyesh P Engineer; Manoj R Gumber; Vivek B Kute; Rajesh Singh; Himanshu V Patel; Aruna V Vanikar; Dinesh Gera; Pankaj R Shah; Hargovind L Trivedi
Journal:  J Nephropharmacol       Date:  2015-11-14
  6 in total

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