JOURNAL ARTICLE

Kindler syndrome with a novel mutation and gynaecological complication.

  • Published In: Clinical & Experimental Dermatology, 2024, v. 49, n. 3. P. 302 1 of 3

  • Database: Academic Search Ultimate 2 of 3

  • Authored By: Tanigassalame, Pavithren; Murthy, Aravind Baskar; Palaniappan, Vijayasankar; Karthikeyan, Kaliaperumal; Kumar, T Senthil 3 of 3

Abstract

Kindler syndrome is a rare genetic skin disorder characterized by skin fragility, blisters, photosensitivity, skin atrophy, and mucosal inflammation. It is a subtype of inherited epidermolysis bullosa and is inherited in an autosomal recessive pattern. This article reports a case of Kindler syndrome in a 40-year-old woman with a giant myometrial cyst and a novel mutation. The article provides a detailed description of the clinical features and genetic basis of Kindler syndrome, as well as the unique complications observed in this particular case. Further research is needed to explore the characteristics of this novel mutation. [Extracted from the article]

Additional Information

  • Source:Clinical & Experimental Dermatology. 2024/03, Vol. 49, Issue 3, p302
  • Document Type:Article
  • Subject Area:Complementary and Alternative Medicine
  • Publication Date:2024
  • ISSN:0307-6938
  • DOI:10.1093/ced/llad364
  • Accession Number:175672547
  • Copyright Statement:Copyright of Clinical & Experimental Dermatology is the property of Oxford University Press / USA and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

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