Literature DB >> 20865259

Winchester syndrome: the progression of radiological findings over a 23-year period.

Radovan Vanatka1, Cécile Rouzier, Jean Claude Lambert, Carole Leroux, Alain Coussement.   

Abstract

Winchester syndrome (WS) is a rare autosomal recessive syndrome resulting in multicentric osteolysis. Only a few cases of WS have been described in the literature worldwide. It has recently been shown to be caused by mutation in the gene encoding matrix metalloproteinase-2 (MMP2). We report a patient affected by WS with a proven mutation of the MMP2 gene and describe the progression of radiological findings over a 23-year period. To our knowledge there is no comparable article concerning the WS in the literature.

Entities:  

Mesh:

Year:  2010        PMID: 20865259     DOI: 10.1007/s00256-010-1033-y

Source DB:  PubMed          Journal:  Skeletal Radiol        ISSN: 0364-2348            Impact factor:   2.199


  6 in total

1.  Progressive multilayered banded skin in Winchester syndrome.

Authors:  Rachel U Sidwell; Louise A Brueton; Sophie A Grabczynska; Nick Francis; Robert C D Staughton
Journal:  J Am Acad Dermatol       Date:  2004-02       Impact factor: 11.527

2.  [Biochemical and ultrastructural study of two familial cases of Winchester syndrome].

Authors:  J C Lambert; J Y Jaffray; J C Michalski; J P Ortonne; V Paquis; A M Saunières
Journal:  J Genet Hum       Date:  1989-09

3.  A new acid mucopolysaccharidosis with skeletal deformities simulating rheumatoid arthritis.

Authors:  P Winchester; H Grossman; W N Lim; B S Danes
Journal:  Am J Roentgenol Radium Ther Nucl Med       Date:  1969-05

4.  Peripheral corneal opacification and skeletal deformities. A newly recognized acid mucopolysaccharidosis simulating rheumatoid arthritis.

Authors:  S I Brown; T Kuwabara
Journal:  Arch Ophthalmol       Date:  1970-06

5.  Torg syndrome is caused by inactivating mutations in MMP2 and is allelic to NAO and Winchester syndrome.

Authors:  Andreas Zankl; Lauren Pachman; Andrew Poznanski; Luisa Bonafé; Fengqiang Wang; Yelena Shusterman; David A Fishman; Andrea Superti-Furga
Journal:  J Bone Miner Res       Date:  2007-02       Impact factor: 6.741

6.  The Winchester syndrome: a nonlysosomal connective tissue disease.

Authors:  D W Hollister; D L Rimoin; R S Lachman; A H Cohen; W B Reed; G W Westin
Journal:  J Pediatr       Date:  1974-05       Impact factor: 4.406

  6 in total
  3 in total

1.  Different roles of matrix metalloproteinase 2 in osteolysis of skeletal dysplasia and bone metastasis (Review).

Authors:  Xiumao Li; Libin Jin; Yanbin Tan
Journal:  Mol Med Rep       Date:  2020-11-25       Impact factor: 2.952

2.  Taurodontism in dental genetics.

Authors:  Manogari Chetty; Imaan A Roomaney; Peter Beighton
Journal:  BDJ Open       Date:  2021-07-09

3.  Multicentric Osteolysis, Nodulosis, and Arthropathy in two unrelated children with matrix metalloproteinase 2 variants: Genetic-skeletal correlations.

Authors:  Hanan Elsebaie; Mohamed Abdelhafiz Mansour; Solaf M Elsayed; Shady Mahmoud; Tamer A El-Sobky
Journal:  Bone Rep       Date:  2021-07-10
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.