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Kindler's syndrome: A rare case report
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...
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| Glavni autori: | , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Medknow Publications & Media Pvt Ltd
2014
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4067787/ https://ncbi.nlm.nih.gov/pubmed/24963250 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0976-237X.132342 |
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