Kindler syndrome: report of two cases Síndrome de Kindler: relato de dois casos
Kindler syndrome is a rare autosomal recessive genodermatosis characterized by trauma-induced blisters, progressive poikiloderma and varying degrees of photosensitivity. In 2003, loss-of-function mutations were identified in the gene KIND1 mapped to chromosome 20p12.3. In this paper, we report Kindl...
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| Main Authors: | , , , , , |
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| Format: | Book |
| Published: |
Sociedade Brasileira de Dermatologia,
2012-10-01T00:00:00Z.
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| Subjects: | |
| Online Access: | Connect to this object online. |
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