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Kindler syndrome: a rare case report from Greece
Kindler syndrome is a rare autosomal recessive inherited disease characterized by infantile acral bullae, progressive poikiloderma, cutaneous atrophy, photosensitivity and various forms of mucosal involvement. In this paper, we report a case of a 49-year-old Greek Caucasian male aiming to emphasize...
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| Foilsithe in: | Oxf Med Case Reports |
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| Main Authors: | , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Oxford University Press
2019
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6396407/ https://ncbi.nlm.nih.gov/pubmed/30838128 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/omcr/omz003 |
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