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[AL amyloidosis].
Rev Med Brux. 2001 Feb; 22(1):9-14.RM

Abstract

AL amyloidosis is a systemic disease caused by the deposition of fibrillar proteins in organs and tissues. These deposits are responsible for organic dysfunctions and may be rapidly lethal. Current therapy is unsatisfactory. We describe three clinical cases of multisystemic AL amyloidosis but with different initial presentation: nephrotic syndrome, cardiac failure and hepatic insufficiency. We review the literature about the clinical features, diagnostic methods and treatment of the disease.

Authors+Show Affiliations

Service de Médecine, H.I.S., Site Joseph Bracops, U.L.B.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
English Abstract
Journal Article

Language

fre

PubMed ID

11252906

Citation

Hedeshi, A R., et al. "[AL Amyloidosis]." Revue Medicale De Bruxelles, vol. 22, no. 1, 2001, pp. 9-14.
Hedeshi AR, Brenez D, Benaddia L, et al. [AL amyloidosis]. Rev Med Brux. 2001;22(1):9-14.
Hedeshi, A. R., Brenez, D., Benaddia, L., Vandervelde, D., Khodadadi, E., Ardichvili, D., & Malarme, M. (2001). [AL amyloidosis]. Revue Medicale De Bruxelles, 22(1), 9-14.
Hedeshi AR, et al. [AL Amyloidosis]. Rev Med Brux. 2001;22(1):9-14. PubMed PMID: 11252906.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [AL amyloidosis]. AU - Hedeshi,A R, AU - Brenez,D, AU - Benaddia,L, AU - Vandervelde,D, AU - Khodadadi,E, AU - Ardichvili,D, AU - Malarme,M, PY - 2001/3/17/pubmed PY - 2001/4/6/medline PY - 2001/3/17/entrez SP - 9 EP - 14 JF - Revue medicale de Bruxelles JO - Rev Med Brux VL - 22 IS - 1 N2 - AL amyloidosis is a systemic disease caused by the deposition of fibrillar proteins in organs and tissues. These deposits are responsible for organic dysfunctions and may be rapidly lethal. Current therapy is unsatisfactory. We describe three clinical cases of multisystemic AL amyloidosis but with different initial presentation: nephrotic syndrome, cardiac failure and hepatic insufficiency. We review the literature about the clinical features, diagnostic methods and treatment of the disease. SN - 0035-3639 UR - https://www.unboundmedicine.com/medline/citation/11252906/[AL_amyloidosis]_ L2 - http://www.diseaseinfosearch.org/result/380 DB - PRIME DP - Unbound Medicine ER -