Literature DB >> 24475416

A renal variant of Fabry disease: A case with a novel Gal A hemizygote mutation.

Jorge H Mukdsi1, Silvina Gutiérrez1, Belén Barrón2, Pablo Novoa2, Segundo Fernández3, Ana B de Diller1, Alicia I Torres1, Richard N Formica4, Marcelo Orías2.   

Abstract

BACKGROUND: Fabry disease is caused by an X-linked recessive inborn error of glycosphingolipid metabolism with deficient activity of a lysosomal enzyme, alpha-galactosidase A (α-GalA). CASE
PRESENTATION: A 46 year-old man with progressive kidney disease showed on kidney biopsy electron microscopic evidence of Fabry disease. The patient had no systemic manifestations of Fabry disease, despite residual α-GalA activity, therefore genetic testing was done by direct DNA sequencing, demonstrating a new GAL A gene mutation (C174G-exon 3). After three years of enzyme replacement therapy (agalsidase beta) treatment, a second biopsy was done. Although there was demonstrable clearance of intracellular inclusions, remarkable podocyte activation was evident.
CONCLUSIONS: This report represents an unusual renal variant of Fabry disease and provides histologic data on long-term follow up after enzyme replacement therapy.

Entities:  

Keywords:  Enzyme replacement therapy; Fabry disease; Kidney electron microscopy

Year:  2012        PMID: 24475416      PMCID: PMC3886146          DOI: 10.5812/nephropathol.8123

Source DB:  PubMed          Journal:  J Nephropathol        ISSN: 2251-8363


  9 in total

1.  Natural history of Fabry renal disease: influence of alpha-galactosidase A activity and genetic mutations on clinical course.

Authors:  Mary H Branton; Raphael Schiffmann; Sharda G Sabnis; Gary J Murray; Jane M Quirk; Gheona Altarescu; Lev Goldfarb; Roscoe O Brady; James E Balow; Howard A Austin Iii; Jeffrey B Kopp
Journal:  Medicine (Baltimore)       Date:  2002-03       Impact factor: 1.889

2.  Alpha-galactosidase activity should be examined in patients with proteinuria: what have we learned from a family affected with Fabry disease?

Authors:  Ni-Chung Lee; Dau-Ming Niu; Ching-Yuang Lin; Kwang-Jen Hsiao; An-Hang Yang; Yee-Yung Ng
Journal:  Nephrol Dial Transplant       Date:  2005-10-12       Impact factor: 5.992

Review 3.  Nephropathy in Fabry disease: the importance of early diagnosis and testing in high-risk populations.

Authors:  Björn Oqvist; Barry M Brenner; João Paulo Oliveira; Alberto Ortiz; Roland Schaefer; Einar Svarstad; Christoph Wanner; Kate Zhang; David G Warnock
Journal:  Nephrol Dial Transplant       Date:  2009-03-16       Impact factor: 5.992

4.  Sustained, long-term renal stabilization after 54 months of agalsidase beta therapy in patients with Fabry disease.

Authors:  Dominique P Germain; Stephen Waldek; Maryam Banikazemi; David A Bushinsky; Joel Charrow; Robert J Desnick; Philip Lee; Thomas Loew; Anouk C Vedder; Rekha Abichandani; William R Wilcox; Nathalie Guffon
Journal:  J Am Soc Nephrol       Date:  2007-04-04       Impact factor: 10.121

5.  Globotriaosylceramide accumulation in the Fabry kidney is cleared from multiple cell types after enzyme replacement therapy.

Authors:  Beth L Thurberg; Helmut Rennke; Robert B Colvin; Steven Dikman; Ronald E Gordon; A Bernard Collins; Robert J Desnick; Michael O'Callaghan
Journal:  Kidney Int       Date:  2002-12       Impact factor: 10.612

6.  Amiodarone pulmonary toxicity: functional and ultrastructural evaluation.

Authors:  F L Liu; R D Cohen; E Downar; J W Butany; J D Edelson; A S Rebuck
Journal:  Thorax       Date:  1986-02       Impact factor: 9.139

7.  Chloroquine-induced lipidosis mimicking Fabry disease.

Authors:  Diana Albay; Sharon G Adler; Jaya Philipose; C C Calescibetta; Stephen G Romansky; Arthur H Cohen
Journal:  Mod Pathol       Date:  2005-05       Impact factor: 7.842

8.  Fabry disease: detection of undiagnosed hemodialysis patients and identification of a "renal variant" phenotype.

Authors:  Shoichiro Nakao; Chihaya Kodama; Toshihiro Takenaka; Akihiro Tanaka; Yuichiro Yasumoto; Aichi Yoshida; Tamotsu Kanzaki; Annette L D Enriquez; Christine M Eng; Hiromitsu Tanaka; Chuwa Tei; Robert J Desnick
Journal:  Kidney Int       Date:  2003-09       Impact factor: 10.612

9.  Recommendations and guidelines for the diagnosis and treatment of Fabry nephropathy in adults.

Authors:  Alberto Ortiz; João P Oliveira; Christoph Wanner; Barry M Brenner; Stephen Waldek; David G Warnock
Journal:  Nat Clin Pract Nephrol       Date:  2008-04-22
  9 in total
  7 in total

1.  Is it or is it not a pathogenic mutation? Is it or is it not the podocyte?

Authors:  Maria Dolores Sanchez-Niño; Alberto Ortiz
Journal:  J Nephropathol       Date:  2012-10-01

2.  The alpha-galactosidase A p.Arg118Cys variant does not cause a Fabry disease phenotype: data from individual patients and family studies.

Authors:  Susana Ferreira; Alberto Ortiz; Dominique P Germain; Miguel Viana-Baptista; António Caldeira-Gomes; Marta Camprecios; Maria Fenollar-Cortés; Ángel Gallegos-Villalobos; Diego Garcia; José Antonio García-Robles; Jesús Egido; Eduardo Gutiérrez-Rivas; José Antonio Herrero; Sebastián Mas; Raluca Oancea; Paloma Péres; Luis Manuel Salazar-Martín; Jesús Solera-Garcia; Helena Alves; Scott C Garman; João Paulo Oliveira
Journal:  Mol Genet Metab       Date:  2014-11-09       Impact factor: 4.797

3.  Fabry disease: the many faces of a single disorder.

Authors:  Roser Torra; Alberto Ortíz
Journal:  Clin Kidney J       Date:  2012-10

4.  A Renal Variant of Fabry Disease Diagnosed by the Presence of Urinary Mulberry Cells.

Authors:  Homare Shimohata; Yujiro Ogawa; Hiroshi Maruyama; Kouichi Hirayama; Masaki Kobayashi
Journal:  Intern Med       Date:  2016-12-01       Impact factor: 1.271

Review 5.  The effect of enzyme replacement therapy on clinical outcomes in male patients with Fabry disease: A systematic literature review by a European panel of experts.

Authors:  Dominique P Germain; Perry M Elliott; Bruno Falissard; Victor V Fomin; Max J Hilz; Ana Jovanovic; Ilkka Kantola; Aleš Linhart; Renzo Mignani; Mehdi Namdar; Albina Nowak; João-Paulo Oliveira; Maurizio Pieroni; Miguel Viana-Baptista; Christoph Wanner; Marco Spada
Journal:  Mol Genet Metab Rep       Date:  2019-02-06

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.  Late onset variants in Fabry disease: Results in high risk population screenings in Argentina.

Authors:  G Serebrinsky; M Calvo; S Fernandez; S Saito; K Ohno; E Wallace; D Warnock; H Sakuraba; J Politei
Journal:  Mol Genet Metab Rep       Date:  2015-06-07
  7 in total

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