Literature DB >> 16680390

Rheumatologic aspects of lysosomal storage diseases.

Bernhard Manger1, Eugen Mengel, Roland M Schaefer.   

Abstract

Lysosomal storage diseases are rare metabolic disorders, some of which can now be treated using enzyme replacement therapies. Because the time point of treatment initiation significantly influences the outcome in Gaucher disease, Fabry disease, and mucopolysaccharidosis type I, early diagnosis is of utmost importance. All three disorders can present with musculoskeletal symptoms in early stages, therefore, the rheumatologist may be the first to be contacted by these patients. Here, we present three characteristic lysosomal storage disease cases to increase awareness in the rheumatological community of the typical symptom constellations associated with these rare but treatable disorders.

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Year:  2006        PMID: 16680390     DOI: 10.1007/s10067-006-0299-x

Source DB:  PubMed          Journal:  Clin Rheumatol        ISSN: 0770-3198            Impact factor:   2.980


  28 in total

1.  Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 60 obligate carrier females.

Authors:  K D MacDermot; A Holmes; A H Miners
Journal:  J Med Genet       Date:  2001-11       Impact factor: 6.318

Review 2.  Enzyme replacement therapy and monitoring for children with type 1 Gaucher disease: consensus recommendations.

Authors:  Joel Charrow; Hans C Andersson; Paige Kaplan; Edwin H Kolodny; Pramod Mistry; Gregory Pastores; Ainu Prakash-Cheng; Barry E Rosenbloom; C Ronald Scott; Rebecca S Wappner; Neal J Weinreb
Journal:  J Pediatr       Date:  2004-01       Impact factor: 4.406

3.  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

4.  Hematologically important mutations: Gaucher disease.

Authors:  E Beutler; T Gelbart
Journal:  Blood Cells Mol Dis       Date:  1998-03       Impact factor: 3.039

Review 5.  [Diagnosis and therapy of Gaucher disease. Current recommendations of German therapy centers in the year 2000].

Authors:  C Niederau; A Rolfs; S vom Dahl; D Häussinger; L W Poll; E Mengel; M Beck
Journal:  Med Klin (Munich)       Date:  2001-01-15

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.  The frequency of lysosomal storage diseases in The Netherlands.

Authors:  B J Poorthuis; R A Wevers; W J Kleijer; J E Groener; J G de Jong; S van Weely; K E Niezen-Koning; O P van Diggelen
Journal:  Hum Genet       Date:  1999 Jul-Aug       Impact factor: 4.132

8.  Replacement therapy for inherited enzyme deficiency--macrophage-targeted glucocerebrosidase for Gaucher's disease.

Authors:  N W Barton; R O Brady; J M Dambrosia; A M Di Bisceglie; S H Doppelt; S C Hill; H J Mankin; G J Murray; R I Parker; C E Argoff
Journal:  N Engl J Med       Date:  1991-05-23       Impact factor: 91.245

9.  Gaucher's disease: a disease with chronic stimulation of the immune system.

Authors:  Y Shoenfeld; L A Gallant; M Shaklai; E Livni; M Djaldetti; J Pinkhas
Journal:  Arch Pathol Lab Med       Date:  1982-08       Impact factor: 5.534

10.  The presenting features of mucopolysaccharidosis type IH (Hurler syndrome).

Authors:  M A Cleary; J E Wraith
Journal:  Acta Paediatr       Date:  1995-03       Impact factor: 2.299

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  5 in total

1.  Isokinetic muscle strength differences in patients with mucopolysaccharidosis I, II, and VI.

Authors:  Natalie E Taylor; Donald R Dengel; Troy C Lund; Kyle D Rudser; Paul J Orchard; Julia Steinberger; Chester B Whitley; Lynda E Polgreen
Journal:  J Pediatr Rehabil Med       Date:  2014

2.  Early diagnosis of fabry disease in a patient with toe tip pain.

Authors:  Ki Bum Park; Kyung Ream Han; Jae Woo Lee; Seung Ho Kim; Do Wan Kim; Chan Kim; Jung Min Ko
Journal:  Korean J Pain       Date:  2010-08-26

Review 3.  Rare monogenetic syndromes in rheumatology practice.

Authors:  K Manger; H Nüsslein; G Schett; B Manger
Journal:  Clin Rheumatol       Date:  2009-02-18       Impact factor: 2.980

4.  The Influence of Patient-Reported Joint Manifestations on Quality of Life in Fabry Patients.

Authors:  Alexandra Ivleva; Ekaterina Weith; Atul Mehta; Derralynn A Hughes
Journal:  JIMD Rep       Date:  2018-01-30

5.  Beyond the guidelines management of juvenile idiopathic arthritis: a case report of a girl with polyarticular disease refractory to multiple treatment options and Leri Weill syndrome.

Authors:  Vana Vukić; Ana Smajo; Mandica Vidović; Rudolf Vukojević; Miroslav Harjaček; Lovro Lamot
Journal:  BMC Pediatr       Date:  2021-01-15       Impact factor: 2.125

  5 in total

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