A preemptive combined liver-kidney transplantation in Aα fibrinogen chain renal amyloidosis;Transplantation préemptive foie-rein pour une amylose rénale à fibrinogène Aα

Nephrologie et Therapeutique

Volumn 5, Issue 2, 2009, Pages 139-143

  Delabre, Jean Philippe ^a   Pageaux, Georges Philippe ^b   Le Quellec, Alain ^b   Raynaud, Pierre ^c   Grateau, Gilles ^d   Mourad, Georges ^a  

^a LAPEYRONIE HOSPITAL   (France)

^b HÔPITAL SAINT ELOI   (France)

^c GUI DE CHAULIAC HOSPITAL   (France)

^d HÔPITAL TENON   (France)

Author keywords

Adult; Amyloidosis; Fibrinogen; Kidney transplantation; Liver transplantation; Renal insufficiency, chronic

Indexed keywords

FIBRINOGEN; FIBRINOGEN A ALPHA; UNCLASSIFIED DRUG;

ADULT; ANAMNESIS; ARTICLE; CASE REPORT; CLINICAL ASSESSMENT; CLINICAL FEATURE; FEMALE; GENE MUTATION; HUMAN; KIDNEY AMYLOIDOSIS; KIDNEY FAILURE; KIDNEY TRANSPLANTATION; LIVER DISEASE; LIVER TRANSPLANTATION; NEPHROTIC SYNDROME; PORTUGAL; RECURRENCE RISK; RISK ASSESSMENT;

ADULT; AMYLOIDOSIS, FAMILIAL; FEMALE; FIBRINOGEN; HUMANS; KIDNEY FAILURE, CHRONIC; KIDNEY TRANSPLANTATION; LIVER TRANSPLANTATION; MUTATION, MISSENSE; PEDIGREE; POINT MUTATION; RECURRENCE;

EID: 63149164241     PISSN: 17697255     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.nephro.2008.08.015     Document Type: Article

References (18)

1. Ostertag B. Demonstration einer eigenartigen amiliaren "paramyloidose". Zentralbl Allg Pathol 56 (1932) 253-254
2. Gillmore J.D., Booth D.R., Rela M., Heaton N.D., Rahman V., Stangou A.J., et al. Curative hepatorenal transplantation in systemic amyloidosis caused by the glu526val fibrinogen alpha-chain variant in an english family. QJM 93 (2000) 269-275
3. Benson M.D., Liepnieks J., Uemichi T., Wheeler G., and Correa R. Hereditary renal amyloidosis associated with a mutant fibrinogen alpha-chain. Nat Genet 3 (1993) 252-255
4. Lachmann H.J., Booth D.R., Booth S.E., Bybee A., Gilbertson J.A., Gillmore J.D., et al. Misdiagnosis of hereditary amyloidosis as al (primary) amyloidosis. N Engl J Med 346 (2002) 1786-1791
5. Uemichi T., Liepnieks J.J., Gertz M.A., and Benson M.D. Fibrinogen A alpha-chain leu 554: an african-american kindred with late onset renal amyloidosis. Amyloid 5 (1998) 188-192
6. Uemichi T., Liepnieks J.J., and Benson M.D. Hereditary renal amyloidosis with a novel variant fibrinogen. J Clin Invest 93 (1994) 731-736
7. Uemichi T., Liepnieks J.J., Yamada T., Gertz M.A., Bang N., and Benson M.D. A frame shift mutation in the fibrinogen A alpha-chain gene in a kindred with renal amyloidosis. Blood 87 (1996) 4197-4203
8. Hamidi Asl L., Liepnieks J.J., Uemichi T., Rebibou J.M., Justrabo E., Droz D., et al. Renal amyloidosis with a frame shift mutation in fibrinogen A alpha-chain gene producing a novel amyloid protein. Blood 90 (1997) 4799-4805
9. Kang H.G., Bybee A., Ha I.S., Park M.S., Gilbertson J.A., Cheong H.I., et al. Hereditary amyloidosis in early childhood associated with a novel insertion-deletion (indel) in the fibrinogen A alpha-chain gene. Kidney Int 68 (2005) 1994-1998
10. Bybee A., Hollenbeck M., Debusmann E., Gopau D., Gilbertson J., and Lachmann H. Hereditary renal amyloidosis in a german family associated with fibrinogen A alpha-chain glu540val. Amyloid and Amyloidosis: Xth International Symposium on Amyloidosis. Tours, France (2004), CRC Press, Boca Raton p. 315
11. Mousson C., Heyd B., Justrabo E., Rebibou J., Tanter Y., Miguet J., et al. Successful hepatorenal transplantation in hereditary amyloidosis caused by a frame-shift mutation in fibrinogen A alpha-chain gene. Am J Transplant 6 (2006) 632-635
12. Zeldenrust S., Gertz M., Uemichi T., Björnsson J., Wiesner R., Schwab T., et al. Orthotopic liver transplantation for hereditary fibrinogen amyloidosis. Transplantation 75 (2003) 560-561
13. Holmgren G., Steen L., Ekstedt J., Groth C.G., Ericzon B.G., Eriksson S., et al. Biochemical effect of liver transplantation in two swedish patients with familial amyloidotic polyneuropathy (fap-met30). Clin Genet 40 (1991) 242-246
14. Alexander F., and Atkins E. Familial renal amyloidosis. Case reports, literature review and classification. Am J Med 59 (1975) 121-128
15. Uemichi T., Liepnieks J.J., Alexander F., and Benson M.D. The molecular basis of renal amyloidosis in irish-american and polish-canadian kindreds. QJM 89 (1996) 745-750
16. Mornaghi R., Rubinstein P., and Franklin E.C. Studies on the pathogenesis of a familial form of renal amyloidosis. Trans Assoc Am Physicians 94 (1981) 211-216
17. Hamidi Asl L., Fournier V., Billerey C., Justrabo E., Chevet D., Droz D., et al. Fibrinogen A alpha-chain mutation (arg554 leu) associated with hereditary renal amyloidosis in a french family. Amyloid 5 (1998) 279-284
18. de Carvalho M., Linke R.P., Domingos F., Evangelista T., Ducla-Soares J.L., Nathrath W.B.J., et al. Mutant fibrinogen A alpha-chain associated with hereditary renal amyloidosis and peripheral neuropathy. Amyloid 11 (2004) 200-207