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Rare case of dysphagia, skin blistering, missing nails in a young boy
Epidermolysis bullosa is a group of genetic disorders with an autosomal dominant or an autosomal recessive mode of inheritance and more than 300 mutations. The disorder is characterized by blistering mucocutaneous lesions and has several varying phenotypes due to anchoring defect between the epiderm...
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| 發表在: | World J Gastrointest Endosc |
|---|---|
| Main Authors: | , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Baishideng Publishing Group Inc
2015
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4325311/ https://ncbi.nlm.nih.gov/pubmed/25685271 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4253/wjge.v7.i2.154 |
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