Literature DB >> 8678572

Olmsted syndrome. Case report and identification of a keratin abnormality.

D W Kress1, M P Seraly, L Falo, B Kim, B V Jegasothy, B Cohen.   

Abstract

BACKGROUND: Olmsted syndrome is a rare disorder characterized by a mutilating palmoplantar keratoderma and periorificial keratotic plaques. It begins in early childhood and is complicated by the development of painful flexion contractures, constrictions, and autoamputations of the digits. Only 11 cases of Olmsted syndrome have been reported to date. However, no biochemical abnormalities in the skin were reported in any of these cases. OBSERVATIONS: We report the 12th case of Olmsted syndrome. In addition, we describe a keratin abnormality found in a skin specimen obtained from our patient. The specimen showed a suprabasilar staining pattern with AE1, an antibody that shows only basilar staining in normal skin.
CONCLUSION: We report the 12th case of Olmsted syndrome, review the literature, and describe a keratin abnormality that was found in our patient's skin specimen.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8678572     DOI: 10.1001/archderm.132.7.797

Source DB:  PubMed          Journal:  Arch Dermatol        ISSN: 0003-987X


  4 in total

1.  Olmsted syndrome.

Authors:  Abdalla M Attia; Ola A Bakry
Journal:  J Dermatol Case Rep       Date:  2013-06-30

2.  TRPV3 mutants causing Olmsted Syndrome induce impaired cell adhesion and nonfunctional lysosomes.

Authors:  Manoj Yadav; Chandan Goswami
Journal:  Channels (Austin)       Date:  2016-10-18       Impact factor: 2.581

Review 3.  Olmsted syndrome: clinical, molecular and therapeutic aspects.

Authors:  Sabine Duchatelet; Alain Hovnanian
Journal:  Orphanet J Rare Dis       Date:  2015-03-17       Impact factor: 4.123

4.  Olmsted syndrome.

Authors:  Pramod Kumar; P K Sharma; H K Kar
Journal:  Indian J Dermatol       Date:  2008       Impact factor: 1.494

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.