Literature DB >> 15852071

[Fabry disease--a diagnostic and therapeutic challenge].

Gunnar Houge1, Alv Johan Skarbøvik.   

Abstract

BACKGROUND: Fabry disease, unlike most other metabolic diseases, is prone to familiar and regional clustering because of X-linked inheritance and normal fertility in affected men. Affected individuals can be offered intravenous enzyme replacement therapy.
MATERIALS AND METHODS: In two counties in western Norway there are 41 affected individuals, giving a minimum prevalence of the disease of 1 in 17,000. The patient material is briefly presented. We discuss some of the administrative and financial challenges that this type of diseases present in our public health system. RESULTS AND
INTERPRETATION: The great variability in disease expression and severity within and between families delays the diagnosis and necessitates a broad clinical follow up of affected persons. A false diagnosis is often made (e.g. MS, irritable colon, a psychiatric disorder, idiopathic hypertrophic cardiomyopathy, or kidney failure). The follow up regime is briefly described, with special emphasis on the practical and financial implications of enzyme replacement therapy in Norway.

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Year:  2005        PMID: 15852071

Source DB:  PubMed          Journal:  Tidsskr Nor Laegeforen        ISSN: 0029-2001


  7 in total

1.  Exocrine pancreatic insufficiency is not a cause of abdominal complaints in patients with Fabry disease.

Authors:  Miroslav Vujasinovic; Bojan Tepes; Bojan Vujkovac; Andreja Cokan Vujkovac; Martin Tretjak; Vesna Korat
Journal:  Wien Klin Wochenschr       Date:  2015-04-03       Impact factor: 1.704

2.  Fabry or not Fabry--a question of ascertainment.

Authors:  Gunnar Houge; Camilla Tøndel; Oyvind Kaarbøe; Asle Hirth; Leif Bostad; Einar Svarstad
Journal:  Eur J Hum Genet       Date:  2011-05-18       Impact factor: 4.246

3.  Arrhythmias in Fabry cardiomyopathy.

Authors:  Deepak Acharya; Peter Robertson; G Neal Kay; Leslie Jackson; David G Warnock; Vance J Plumb; José A Tallaj
Journal:  Clin Cardiol       Date:  2012-08-09       Impact factor: 2.882

Review 4.  Genetics of cerebral small vessel disease.

Authors:  Jay Chol Choi
Journal:  J Stroke       Date:  2015-01-30       Impact factor: 6.967

5.  Lentivector Iterations and Pre-Clinical Scale-Up/Toxicity Testing: Targeting Mobilized CD34+ Cells for Correction of Fabry Disease.

Authors:  Ju Huang; Aneal Khan; Bryan C Au; Dwayne L Barber; Lucía López-Vásquez; Nicole L Prokopishyn; Michel Boutin; Michael Rothe; Jack W Rip; Mona Abaoui; Murtaza S Nagree; Shaalee Dworski; Axel Schambach; Armand Keating; Michael L West; John Klassen; Patricia V Turner; Sandra Sirrs; C Anthony Rupar; Christiane Auray-Blais; Ronan Foley; Jeffrey A Medin
Journal:  Mol Ther Methods Clin Dev       Date:  2017-05-12       Impact factor: 6.698

Review 6.  Genetic Factors of Cerebral Small Vessel Disease and Their Potential Clinical Outcome.

Authors:  Vo Van Giau; Eva Bagyinszky; Young Chul Youn; Seong Soo A An; Sang Yun Kim
Journal:  Int J Mol Sci       Date:  2019-09-03       Impact factor: 5.923

7.  Global research on Fabry's disease: Demands for a rare disease.

Authors:  Doris Klingelhöfer; Markus Braun; Rebekka K Seeger-Zybok; David Quarcoo; Dörthe Brüggmann; David A Groneberg
Journal:  Mol Genet Genomic Med       Date:  2020-02-07       Impact factor: 2.183

  7 in total

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