Kindler syndrome - a rare type of hereditary epidermolysis bullosa
The Kindler syndrome is one of the types of hereditary epidermolysis bullosa with its onset related to mutations of the KIND1 gene. The authors describe a case of a family with three members suffering from this rare disease. All of these patients have typical clinical manifestations of the Kindler s...
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| Hlavní autoři: | , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
State Scientific Center of Dermatovenereology and Cosmetology
2017-08-01
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| Edice: | Vestnik Dermatologii i Venerologii |
| Témata: | |
| On-line přístup: | https://www.vestnikdv.ru/jour/article/view/167 |
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