Literature DB >> 29657451

Total hip arthroplasty in Hurler syndrome - 8 years follow up - A case report with review of literature.

Deepak Gautam1, Rajesh Malhotra1.   

Abstract

Life expectancy in Hurler syndrome is significantly improved by enzyme therapy with bone marrow transplantation. However, the deterioration of skeletal abnormalities persists. Hip dysplasia is a common presentation which may progress to significant hip arthritis requiring total hip arthroplasty at later stage. We report a long-term outcome of cementless total hip arthroplasty in a patient with Hurler syndrome who was successfully treated with bone marrow transplant.

Entities:  

Keywords:  Hurler syndrome; Mucopolysaccharidosis; Total hip arthroplasty

Year:  2018        PMID: 29657451      PMCID: PMC5895911          DOI: 10.1016/j.jor.2018.01.036

Source DB:  PubMed          Journal:  J Orthop        ISSN: 0972-978X


  10 in total

1.  Musculoskeletal manifestations of Hurler syndrome: long-term follow-up after bone marrow transplantation.

Authors:  Jason S Weisstein; Eliana Delgado; Lynne S Steinbach; Kim Hart; Seymour Packman
Journal:  J Pediatr Orthop       Date:  2004 Jan-Feb       Impact factor: 2.324

2.  Total hip arthroplasty in very young bone marrow transplant patients.

Authors:  Cameron K Ledford; Alexander R Vap; Michael P Bolognesi; Samuel S Wellman
Journal:  J Surg Orthop Adv       Date:  2015

3.  Relative frequency of the Hurler and Hunter syndromes.

Authors:  R B Lowry; D H Renwick
Journal:  N Engl J Med       Date:  1971-01-28       Impact factor: 91.245

4.  A Long-term Retrospective Evaluation of Functional and Radiographic Outcomes of Pediatric Hip Surgery in Hurler Syndrome.

Authors:  Jim Kennedy; Jacques Noel; Anne O'Meara; Kevin Mulhall; Ellen Crushell; Esmond Fogarty; Paula Kelly
Journal:  J Pediatr Orthop       Date:  2016-01       Impact factor: 2.324

5.  Reversal of clinical features of Hurler's disease and biochemical improvement after treatment by bone-marrow transplantation.

Authors:  J R Hobbs; K Hugh-Jones; A J Barrett; N Byrom; D Chambers; K Henry; D C James; C F Lucas; T R Rogers; P F Benson; L R Tansley; A D Patrick; J Mossman; E P Young
Journal:  Lancet       Date:  1981-10-03       Impact factor: 79.321

6.  Progression of Hip Dysplasia in Mucopolysaccharidosis Type I Hurler After Successful Hematopoietic Stem Cell Transplantation.

Authors:  Eveline J Langereis; Matthijs M den Os; Catherine Breen; Simon A Jones; Olga C Knaven; Jean Mercer; Weston P Miller; Paula M Kelly; Jim Kennedy; Tyler G Ketterl; Anne O'Meara; Paul J Orchard; Troy C Lund; Rick R van Rijn; Ralph J Sakkers; Klane K White; Frits A Wijburg
Journal:  J Bone Joint Surg Am       Date:  2016-03-02       Impact factor: 5.284

7.  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

8.  Musculoskeletal manifestations in mucopolysaccharidosis type I (Hurler syndrome) following hematopoietic stem cell transplantation.

Authors:  Mona Schmidt; Sandra Breyer; Ulrike Löbel; Sinef Yarar; Ralf Stücker; Kurt Ullrich; Ingo Müller; Nicole Muschol
Journal:  Orphanet J Rare Dis       Date:  2016-07-08       Impact factor: 4.123

9.  Total Hip Arthroplasty in Mucopolysaccharidosis Type IH.

Authors:  S O'heireamhoin; T Bayer; K J Mulhall
Journal:  Case Rep Orthop       Date:  2012-01-26

Review 10.  Treatment of hip dysplasia in patients with mucopolysaccharidosis type I after hematopoietic stem cell transplantation: results of an international consensus procedure.

Authors:  Eveline J Langereis; Andrea Borgo; Ellen Crushell; Paul R Harmatz; Peter M van Hasselt; Simon A Jones; Paula M Kelly; Christina Lampe; Johanna H van der Lee; Thierry Odent; Ralph Sakkers; Maurizio Scarpa; Matthias U Schafroth; Peter A Struijs; Vassili Valayannopoulos; Klane K White; Frits A Wijburg
Journal:  Orphanet J Rare Dis       Date:  2013-10-03       Impact factor: 4.123

  10 in total
  1 in total

Review 1.  Pain in Mucopolysaccharidoses: Analysis of the Problem and Possible Treatments.

Authors:  Sabrina Congedi; Marcello Orzalesi; Chiara Di Pede; Franca Benini
Journal:  Int J Mol Sci       Date:  2018-10-08       Impact factor: 5.923

  1 in total

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