Literature DB >> 7329476

Hereditary nephritis associated with May-Hegglin anomaly.

F Brivet, R Girot, C Barbanel, C Gazengel, M Maier, J Crosnier.   

Abstract

Hereditary nephritis associated with hematologic abnormalities seems to be an exceptional occurrence. We have observed a family which nephritis was combined with May-Hegglin anomaly. A girl and her father suffered from proteinuria; a paternal uncle received kidney graft; a paternal grand aunt died on periodic hemodialysis. The girl, the father and the uncle presented macrothrombocytopenia (40-100 X 10(9)/l, size 4-8 mum) with prolonged bleeding time (which precluded renal biopsy) and cytoplasmic inclusions in neutrophils (Döhle bodies). These hematologic abnormalities characterize the May-Hegglin anomaly. This kind of association has not been reported so far.

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Year:  1981        PMID: 7329476     DOI: 10.1159/000182240

Source DB:  PubMed          Journal:  Nephron        ISSN: 1660-8151            Impact factor:   2.847


  7 in total

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2.  Sebastian platelet syndrome: a new variant of hereditary macrothrombocytopenia with leukocyte inclusions.

Authors:  A Greinacher; H K Nieuwenhuis; J G White
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3.  Hereditary types of thrombocytopenia with giant platelets and inclusion bodies in the leukocytes.

Authors:  A Greinacher; C Mueller-Eckhardt
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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
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Review 6.  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

7.  Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome?

Authors:  J J Jonsson; A Renieri; P G Gallagher; C E Kashtan; E M Cherniske; M Bruttini; M Piccini; F Vitelli; A Ballabio; B R Pober
Journal:  J Med Genet       Date:  1998-04       Impact factor: 6.318

  7 in total

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