Literature DB >> 6769383

Myelopathy in mucopolysaccharidosis type II (Hunter syndrome).

C E Ballenger, T R Swift, R T Leshner, T A El Gammal, T F McDonald.   

Abstract

A 24-year-old man with Hunter syndrome had spastic quadriparesis due to impingement of thickened meninges upon the cervical spinal cord. Tracheal narrowing due to submucosal deposits (presumably mucopolysaccharide) produced serious ventilatory complications during induction of anesthesia and necessitated tracheostomy before surgical decompression of the spinal cord could be attempted. Recognition of compressive myelopathy and tracheal compromise as late complications of Hunter syndrome may promote early therapy and prevent respiratory catastrophe.

Entities:  

Mesh:

Year:  1980        PMID: 6769383     DOI: 10.1002/ana.410070418

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  8 in total

1.  A clinical and genetic study of Hunter's syndrome. 2. Differences between the mild and severe forms.

Authors:  I D Young; P S Harper; R G Newcombe; I M Archer
Journal:  J Med Genet       Date:  1982-12       Impact factor: 6.318

Review 2.  Spinal meningeal malformations in children (without meningoceles or meningomyeloceles).

Authors:  J Richaud
Journal:  Childs Nerv Syst       Date:  1988-04       Impact factor: 1.475

Review 3.  Neurological findings in Hunter disease: pathology and possible therapeutic effects reviewed.

Authors:  S Al Sawaf; E Mayatepek; B Hoffmann
Journal:  J Inherit Metab Dis       Date:  2008-07-13       Impact factor: 4.982

4.  Mild form of Hunter's syndrome: clinical delineation based on 31 cases.

Authors:  I D Young; P S Harper
Journal:  Arch Dis Child       Date:  1982-11       Impact factor: 3.791

5.  Chiari 1 malformation and holocord syringomyelia in hunter syndrome.

Authors:  Renzo Manara; Daniela Concolino; Angelica Rampazzo; Alessandra Zanetti; Rossella Tomanin; Roberto Faggin; Maurizio Scarpa
Journal:  JIMD Rep       Date:  2013-07-02

6.  Narrow trachea in mucopolysaccharidoses.

Authors:  M E Peters; S Arya; L O Langer; E F Gilbert; R Carlson; W Adkins
Journal:  Pediatr Radiol       Date:  1985

7.  Neurogenic bladder in Hunter's syndrome.

Authors:  K Koyama; Y Moda; A Sone; H Tanaka; Y Hino
Journal:  J Med Genet       Date:  1994-03       Impact factor: 6.318

8.  Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease.

Authors:  Maurizio Scarpa; Zsuzsanna Almássy; Michael Beck; Olaf Bodamer; Iain A Bruce; Linda De Meirleir; Nathalie Guffon; Encarna Guillén-Navarro; Pauline Hensman; Simon Jones; Wolfgang Kamin; Christoph Kampmann; Christina Lampe; Christine A Lavery; Elisa Leão Teles; Bianca Link; Allan M Lund; Gunilla Malm; Susanne Pitz; Michael Rothera; Catherine Stewart; Anna Tylki-Szymańska; Ans van der Ploeg; Robert Walker; Jiri Zeman; James E Wraith
Journal:  Orphanet J Rare Dis       Date:  2011-11-07       Impact factor: 4.123

  8 in total

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