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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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| Publicat a: | BMC Neurol |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2019
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| Matèries: | |
| Accés en línia: | 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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