Literature DB >> 3099372

[Fabry's disease. Rare etiology of a long-term inflammatory syndrome. Apropos of a case].

J J Dubost, B Sauvezie, B Galtier, J Tixeron, S Rampon.   

Abstract

A man aged 54 years presented multiple symptoms (acroparesthesia, familial deafness, cardiomyopathy, diarrhea, adenopathy with infiltration of frothy macrophages, pancytopenia with a dense marrow, chronic meningitis, renal failure) associated with intermittent fever, with feverish attacks and a temperature of 40 degrees C, and with a severe biologic febrile syndrome. Fabry's disease was diagnosed only after 3 years of fruitless explorations. The reasons for this delay are analysed and it is suggested than Fabry's disease be added to the list of conditions responsible for fever or for a persistent inflammatory syndrome.

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Year:  1986        PMID: 3099372

Source DB:  PubMed          Journal:  Rev Rhum Mal Osteoartic        ISSN: 0035-2659


  1 in total

1.  Polyarteritis nodosa-like necrotizing vasculitis in Fabry disease.

Authors:  C B Drachenberg; E J Schweitzer; S T Bartlett; M T Behrens; J C Papadimitriou
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

  1 in total

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