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Parkes Weber syndrome presenting as Stewart-Bluefarb acroangiodermatitis
Parkes Weber syndrome (PWS) is a rare disorder characterised by arteriovenous (AV) fistula, along with capillary, lymphatic, venous malformations and limb hypertrophy. Stewart-Bluefarb syndrome is a variant of acroangiodermatitis, which is associated with congenital AV malformation/fistulas. It usua...
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| Vydáno v: | BMJ Case Rep |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMJ Publishing Group
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6424474/ https://ncbi.nlm.nih.gov/pubmed/30852501 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2018-227793 |
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