Winchester syndrome: Difference between revisions

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'''''Synonyms and keywords:''''' Torg-Winchester syndrome
'''''Synonyms and keywords:''''' Torg-Winchester syndrome, Nodulosis-arthropathy-osteolysis syndrome
==Overview==
==Overview==
'''Winchester syndrome''' in a rare [[congenital disorder|congenital]] [[connective tissue disease]].
'''Winchester syndrome''' in a rare [[congenital disorder|congenital]] [[connective tissue disease]].

Revision as of 13:22, 27 July 2012

Torg-Winchester syndrome
Matrix Metalloproteinase 2
OMIM 259600

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2]

Synonyms and keywords: Torg-Winchester syndrome, Nodulosis-arthropathy-osteolysis syndrome

Overview

Winchester syndrome in a rare congenital connective tissue disease.

Historical perspective

It was first described in 1969.

Pathophysiology

In 2005 a patient with Winchester syndrome was shown to have mutations in the matrix metalloproteinase 2 (MMP2) gene.[1] A 2006 study showed other mutations in the same gene, and observed that Winchester syndrome is probably part of a continuum that also includesTorg syndrome and nodulosis-arthropathy-osteolysis syndrome (NAO).[2]

Differentiating from other diseases

Winchester syndrome should be differentiated from rheumatoid arthritis.[3]

Diagnosis

The main characteristics are short stature, marked contractures of joints, opacities in the cornea, a coarse face, dissolution of the carpal and tarsal bones (in the hands and feet respectively) and osteoporosis. Increased uronic acid was demonstrated in cultured fibroblasts from the skin and to a lesser degree in both parents. Despite initial tests not showing increased mucopolysaccharide excretion, the disease was regarded as a mucopolysaccharidosis.[3]

References

  1. Zankl A, Bonafé L, Calcaterra V, Di Rocco M, Superti-Furga A (2005). "Winchester syndrome caused by a homozygous mutation affecting the active site of matrix metalloproteinase 2". Clin. Genet. 67 (3): 261–6. doi:10.1111/j.1399-0004.2004.00402.x. PMID 15691365.
  2. Rouzier C, Vanatka R, Bannwarth S; et al. (2006). "A novel homozygous MMP2 mutation in a family with Winchester syndrome". Clin. Genet. 69 (3): 271–6. doi:10.1111/j.1399-0004.2006.00584.x. PMID 16542393.
  3. 3.0 3.1 Winchester P, Grossman H, Lim WN, Danes BS (1969). "A new acid mucopolysaccharidosis with skeletal deformities simulating rheumatoid arthritis". Am J Roentgenol Radium Ther Nucl Med. 106 (1): 121–8. PMID 4238825.

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