Skip to main content
Log in

Renal disease in Fabry patients

  • Published:
Journal of Inherited Metabolic Disease

Abstract

Renal dysfunction is a major complication in hemizygous males with Fabry disease. This often results in end-stage renal failure (ESRF), requiring dialysis or transplantation, on average 10 years after the start of renal impairment. ESRF usually occurs between 40 and 50 years of age, but may occur much earlier. Although progression of renal disease can be rapid, it is variable and may depend on whether there is residual α-galactosidase enzyme activity and on environmental or genetic factors. Significant renal disease is much less common in women carriers of the disease. However, renal changes do occur, which may progress to ESRF as in male patients.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

REFERENCES

  • Branton MH, Schiffmann R, Murray GJ, et al (2000) α-Galactosidase A activity influences renal disease course in Fabry disease. J Am Soc Nephrol 11: 403A (A2113).

    Google Scholar 

  • Colombi A, Kostyal A, Bracher R, et al (1967) Angiokeratoma corporis diffusum-Fabry's disease. Helv Med Acta 34: 67–83.

    PubMed  CAS  Google Scholar 

  • Desnick RJ (2001) Fabry disease: clinical features and recent advances in enzyme replacement therapy. Adv Nephrol 31 (in press).

  • Grünfeld JP, Le Porrier M, Droz D, Bensaude I, Hinglais N, Crosnier J (1975) La transplantation rénale chez les sujets atteints de maladie de Fabry. Transplantation du rein d'un sujet hétérozyogote à un sujet sain. Nouv Presse Méd 4: 2081–2085.

    PubMed  Google Scholar 

  • Gubler MC, Lenoir G, Grünfeld JP, Ulmann A, Droz D, Habib R (1978) Early renal changes in hemizygous and heterozygous patients with Fabry's disease. Kidney Int 13: 223–235.

    PubMed  CAS  Google Scholar 

  • Hillsley RE, Hernandez E, Steenbergen C, Bashore TM, Harrison JK (1995) Inherited restrictive cardiomyopathy in a 74-year-old woman: a case of Fabry's disease. Am Heart J 129: 199–202.

    Article  PubMed  CAS  Google Scholar 

  • Maizel SE, Simmons RL, Kjellstrand C, Fryd DS (1981) Ten-year experience in renal transplantation for Fabry's disease. Transplant Proc 13: 57–59.

    PubMed  CAS  Google Scholar 

  • Muto H, Konoshita T, Nomura H, et al (2000) Fabry disease in patients with end-stage renal disease of unknown etiology. J Am Soc Nephrol 11: 411A.

    Google Scholar 

  • Perdu J, Joly D, Lidove O (1998) Oedème pulmonaire aigu fébrile chez un hémodialysé. Méd Thérap 4: 675–680.

    Google Scholar 

  • Popli S, Molnar, ZV, Leehey, et al (1987) Involvement of renal allograft by Fabry's disease. Am J Nephrol 7: 316–318.

    Article  PubMed  CAS  Google Scholar 

  • Singh HK, Nickeleit V, Kriegsmann J, Harris AA, Jennette JC, Mihatsch MJ (2001) Coexistence of Fabry's disease and necrotizing and crescentic glomerulonephritis. Clin Nephrol 55: 73–79.

    PubMed  CAS  Google Scholar 

  • US Renal Data System (2000) 2000 Annual Data Report. Transplantation. Bethesda: National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Disease.

    Google Scholar 

  • Tognoni, G (1996) ERA-EDTA Registry. Report on management of renal failure in Europe, XXVI, 1995. Nephrol Dial Transplant 11: 1–32.

    Google Scholar 

  • Tsakiris D, Simpson HKL, Jones EHP, et al. (1996) Rare diseases in renal replacement therapy in the ERA-EDTA Registry. Nephrol Dial Transplant 11: 4–20.

    PubMed  Google Scholar 

  • Voglino A, Paradisi M, Dompe G, Onetti Muda A, Faraggiana T (1988) Angiokeratoma corporis diffusum (Fabry's disease) with unusual features in a female patient. Light-and electronmicroscopic investigation. Am J Dermatopathol 10: 343–348.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Grünfeld, JP., Lidove, O., Joly, D. et al. Renal disease in Fabry patients. J Inherit Metab Dis 24 (Suppl 2), 71–74 (2001). https://doi.org/10.1023/A:1012475908718

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1012475908718

Keywords

Navigation