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Degos disease – malignant atrophic papulosis or cutaneointestinal lethal syndrome: rarity of the disease
BACKGROUND: Degos disease is a very rare syndrome with a rare type of multisystem vasculopathy of unknown cause that affects the skin, gastrointestinal tract, and central nervous system. Other organs such as the kidneys, lungs, pleura, liver, heart, and eyes, can also be involved. OBJECTIVE: To high...
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| Vydáno v: | Clin Exp Gastroenterol |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Dove Medical Press
2015
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4403817/ https://ncbi.nlm.nih.gov/pubmed/25926751 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/CEG.S59794 |
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