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CASE REPORT
Year : 2014  |  Volume : 5  |  Issue : 2  |  Page : 217-220

Kindler's syndrome: A rare case report


1 Department of Prosthodontics, SGRD Institute of Dental Sciences and Research, Amritsar, Punjab, India
2 Department of Periodontics, SGRD Institute of Dental Sciences and Research, Amritsar, Punjab, India

Correspondence Address:
Neelam Suman
Department of Prosthodontics, SGRD Institute of Dental Sciences and Research, Amritsar, Punjab
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0976-237X.132342

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Kindler syndrome is a rare hereditary disorder, associated with skin fragility. The syndrome involves the skin and mucous membrane with radiological changes. The genetic defect has been identified on the short arm of chromosome 20. This report describes a 16-year-old patient with classical features like blistering and photosensitivity in childhood and the subsequent development of poikiloderma.


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