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Idiopathic inflammatory myopathy comorbid with Sturge-Weber syndrome: a case report
BACKGROUND: Sturge-Weber syndrome (SWS) is a rare and sporadic congenital neurocutaneous disorder, that is characterized by facial venous capillary malformation (port-wine birthmark), leptomeningeal venous malformation (angiomatosis), glaucoma, and neurologic problems. SWS can comorbid with other di...
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| 發表在: | BMC Neurol |
|---|---|
| Main Authors: | , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
BioMed Central
2019
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6500033/ https://ncbi.nlm.nih.gov/pubmed/31053110 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12883-019-1303-9 |
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