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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Detalles Bibliográficos
Autores principales: Deng, Li, Wang, Dongmei, Ruan, Ni, Fu, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6500033/
https://www.ncbi.nlm.nih.gov/pubmed/31053110
http://dx.doi.org/10.1186/s12883-019-1303-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6500033/
https://www.ncbi.nlm.nih.gov/pubmed/31053110
http://dx.doi.org/10.1186/s12883-019-1303-9

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