Literature DB >> 10079781

Gaucher's disease with valve calcification: possible role of Gaucher cells, bone matrix proteins and integrins.

J P Veinot1, D Elstein, D Hanania, A Abrahamov, S Srivatsa, A Zimran.   

Abstract

Gaucher's disease, an autosomal recessive storage disease, leads to deposition of glucocerebrosides in various organs, especially those of the reticuloendothelial system. The heart is not thought to be frequently involved and studies of patients with cardiac involvement have concentrated on myocardial involvement. Despite careful prior investigation Gaucher cells have never been detected in the valves of these patients. Pathological findings of a patient with Gaucher's disease, type IIIc, with prominent cardiac valvular involvement are reported and, for the first time, the presence of Gaucher cells in the valve tissue is documented. There is evidence that the pathogenesis of the valvular injury may be by way of a cell-mediated mechanism involving bone matrix proteins and integrins.

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Year:  1999        PMID: 10079781

Source DB:  PubMed          Journal:  Can J Cardiol        ISSN: 0828-282X            Impact factor:   5.223


  5 in total

1.  Gaucher's disease type III C: Unusual cause of intracardiac calcification.

Authors:  Sejal Shah; Amit Misri; Meenakshi Bhat; Sunita Maheshwari
Journal:  Ann Pediatr Cardiol       Date:  2008-07

2.  Echocardiographic Assessment of Left Ventricular Function in Type 1 Gaucher's Disease.

Authors:  Mirta Kozelj; Samo Zver; Vesna Zadnik
Journal:  Adv Hematol       Date:  2010-07-20

3.  Vitamin D receptor (VDR) polymorphisms in the cardiac variant of Gaucher disease.

Authors:  Allen Greenwood; Gheona Altarescu; Ari Zimran; Deborah Elstein
Journal:  Pediatr Cardiol       Date:  2009-09-26       Impact factor: 1.655

4.  Mitral valve prolapse and mitral insufficiency in two siblings with Gaucher's disease.

Authors:  S Celik; C Erdol; M Baykan; M Gokce; C Orem; I Durmus
Journal:  Images Paediatr Cardiol       Date:  2000-07

5.  Aortic calcification in Gaucher disease: a case report.

Authors:  Saud Alsahli; Dalal K Bubshait; Zuhair A Rahbeeni; Majid Alfadhel
Journal:  Appl Clin Genet       Date:  2018-10-17
  5 in total

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