Literature DB >> 23052995

[Fabry disease : diagnosis and treatment].

N Üçeyler1, C Sommer.   

Abstract

Fabry disease is an X-linked hereditary lysosomal storage disorder with deficiency of the enzyme α-galactosidase A and lysosomal deposits of the glycosphingolipid globotriaosylceramid-3 (Gb-3). Males are predominantly affected by this multisystem disorder; however, females may develop any grade of disease severity. Cardiac, renal, and cerebral involvement may be life limiting-the latter due to stroke in young age. The peripheral nervous system is affected in terms of small fiber neuropathy with characteristic heat-induced acral pain. Pain is the most frequent first symptom of Fabry disease, but is often misjudged and undertreated. Enzyme replacement therapy is available as a treatment option. Fabry-associated pain is treated following the principles of analgesic treatment in neuropathic pain conditions, but some special features need to be considered and will be discussed.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 23052995     DOI: 10.1007/s00482-012-1238-1

Source DB:  PubMed          Journal:  Schmerz        ISSN: 0932-433X            Impact factor:   1.107


  20 in total

1.  Enzyme replacement therapy improves peripheral nerve and sweat function in Fabry disease.

Authors:  Raphael Schiffmann; Mary Kay Floeter; James M Dambrosia; Surya Gupta; David F Moore; Yehonatan Sharabi; Ramesh K Khurana; Roscoe O Brady
Journal:  Muscle Nerve       Date:  2003-12       Impact factor: 3.217

Review 2.  Enzyme replacement therapy for Fabry disease: lessons from two alpha-galactosidase A orphan products and one FDA approval.

Authors:  Robert J Desnick
Journal:  Expert Opin Biol Ther       Date:  2004-07       Impact factor: 4.388

Review 3.  Enzyme replacement therapy for Anderson-Fabry disease.

Authors:  Regina P El Dib; Gregory M Pastores
Journal:  Cochrane Database Syst Rev       Date:  2010-05-12

4.  Safety and efficacy of recombinant human alpha-galactosidase A replacement therapy in Fabry's disease.

Authors:  C M Eng; N Guffon; W R Wilcox; D P Germain; P Lee; S Waldek; L Caplan; G E Linthorst; R J Desnick
Journal:  N Engl J Med       Date:  2001-07-05       Impact factor: 91.245

5.  Fabry-database.org: database of the clinical phenotypes, genotypes and mutant α-galactosidase A structures in Fabry disease.

Authors:  Seiji Saito; Kazuki Ohno; Hitoshi Sakuraba
Journal:  J Hum Genet       Date:  2011-03-17       Impact factor: 3.172

6.  Enzyme replacement therapy in Fabry disease: a randomized controlled trial.

Authors:  R Schiffmann; J B Kopp; H A Austin; S Sabnis; D F Moore; T Weibel; J E Balow; R O Brady
Journal:  JAMA       Date:  2001-06-06       Impact factor: 56.272

7.  A phase 1/2 clinical trial of enzyme replacement in fabry disease: pharmacokinetic, substrate clearance, and safety studies.

Authors:  C M Eng; M Banikazemi; R E Gordon; M Goldman; R Phelps; L Kim; A Gass; J Winston; S Dikman; J T Fallon; S Brodie; C B Stacy; D Mehta; R Parsons; K Norton; M O'Callaghan; R J Desnick
Journal:  Am J Hum Genet       Date:  2001-02-01       Impact factor: 11.025

8.  Enzyme replacement therapy with agalsidase alfa in patients with Fabry's disease: an analysis of registry data.

Authors:  A Mehta; M Beck; P Elliott; R Giugliani; A Linhart; G Sunder-Plassmann; R Schiffmann; F Barbey; M Ries; J T R Clarke
Journal:  Lancet       Date:  2009-12-12       Impact factor: 79.321

Review 9.  Fabry disease.

Authors:  Dominique P Germain
Journal:  Orphanet J Rare Dis       Date:  2010-11-22       Impact factor: 4.123

10.  Use of gabapentin to reduce chronic neuropathic pain in Fabry disease.

Authors:  M Ries; E Mengel; G Kutschke; K S Kim; F Birklein; F Krummenauer; M Beck
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.750

View more
  1 in total

1.  Gene variants of unknown significance in Fabry disease: Clinical characteristics of c.376A>G (p.Ser126Gly).

Authors:  Kolja Lau; Nurcan Üçeyler; Tereza Cairns; Lora Lorenz; Claudia Sommer; Magnus Schindehütte; Kerstin Amann; Christoph Wanner; Peter Nordbeck
Journal:  Mol Genet Genomic Med       Date:  2022-02-25       Impact factor: 2.473

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.