Literature DB >> 11314421

Hurler syndrome: a case report.

S Thomas1, S Tandon.   

Abstract

Hurler syndrome is an inherited disorder of mucopolysaceharide metabolism, which is caused by a defect in genetically controlled pathways of lysosomal degradation. It represents the classical prototype of mucopolysaccharide disorder. An interesting case of a three and a half-year old boy with a rare combination of skeletal, neurological, ophthalmologic, and dental findings is presented. It is a rare syndrome with a very low prevalence of 1:100,000 births and as such the clinician should be aware of this syndrome.

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Year:  2000        PMID: 11314421     DOI: 10.17796/jcpd.24.4.ku653u75nv5vt735

Source DB:  PubMed          Journal:  J Clin Pediatr Dent        ISSN: 1053-4628            Impact factor:   1.065


  4 in total

1.  The oral health needs of children, adolescents and young adults affected by a mucopolysaccharide disorder.

Authors:  Alison James; Christian J Hendriksz; Owen Addison
Journal:  JIMD Rep       Date:  2011-09-06

2.  Hurler syndrome: orofacial, dental, and skeletal findings of a case.

Authors:  Arpita Rai Thakur; Venkatesh G Naikmasur; Atul Sattur
Journal:  Skeletal Radiol       Date:  2014-08-20       Impact factor: 2.199

Review 3.  Gingival enlargements: Differential diagnosis and review of literature.

Authors:  Amit Arvind Agrawal
Journal:  World J Clin Cases       Date:  2015-09-16       Impact factor: 1.337

4.  Clinical manifestation of Hurler syndrome in a 7 year old child.

Authors:  S Sharma; J R Sabharwal; P Datta; S Sood
Journal:  Contemp Clin Dent       Date:  2012-01
  4 in total

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