Idiopathic inflammatory myopathy comorbid with Sturge-Weber syndrome: a case report
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),General Medicine
Link
http://link.springer.com/content/pdf/10.1186/s12883-019-1303-9.pdf
Reference16 articles.
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2. Shirley MD, Tang H, Gallione CJ, Baugher JD, Frelin LP, Cohen B, North PE, Marchuk DA, Comi AM, Pevsner J. Sturge-weber syndrome and port-wine stains caused by somatic mutation in GNAQ. N Engl J Med. 2013;368(21):1971–9.
3. Lo W, Marchuk DA, Ball KL, Juhasz C, Jordan LC, Ewen JB, Comi A, Brain Vascular Malformation Consortium National Sturge-Weber Syndrome W. Updates and future horizons on the understanding, diagnosis, and treatment of Sturge-weber syndrome brain involvement. Dev Med Child Neurol. 2012;54(3):214–23.
4. Schmidt J. Current classification and Management of Inflammatory Myopathies. J Neuromuscul Dis. 2018;5(2):109–29.
5. Selva-O'Callaghan A, Pinal-Fernandez I, Trallero-Araguas E, Milisenda JC, Grau-Junyent JM, Mammen AL. Classification and management of adult inflammatory myopathies. Lancet Neurol. 2018;17(9):816–28.
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