Sturge-Weber syndrome in children. Clinical features, diagnosis and approaches to therapy on the example of three clinical cases-Reference-Cited by-同舟云学术

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Sturge-Weber syndrome in children. Clinical features, diagnosis and approaches to therapy on the example of three clinical cases

Published:2019 Issue:11 Volume:119 Page:55
ISSN:1997-7298
Container-title:Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova
language:en
Short-container-title:Z. nevrol. psikhiatr. im. S.S. Korsakova

Author:

Shchederkina I. O.,Livshtz M. I.,Kuzmina E. V.,Seliverstova E. V.,Kessel A. E.,Petryaykina E. E.

Publisher

Media Sphere Publishing Group

Subject

Psychiatry and Mental health,Neurology (clinical)

Reference45 articles.

1. Shirley MD, Tang H, Gallione CJ. Sturge-Weber syndrome and port-wine stains caused by somatic mutation in GNAQ. N Engl J Med. 2013;268(21):1971-1979.

2. Sturge W. A case of partial epilepsy, apparently due to lesion of one the vasomotor centers of the brain. Transactions of the Clinical Society of London. 1879;12:162.

3. Weber FP. Right-sided hemi-hypotrophy resulting from right-sided congenital spastic hemiplegia, with a morbid condition of the left side of the brain, revealed by radiograms. J Neurol Psychopathol. 1922;3(10):134-139.

4. Weber F. Rare diseases and some debatable subjects. London: Staples Press; 1946.

5. Comi AM. Update on Sturge-Weber syndrome: diagnosis,treatment, quantitative measures, and controversies. Lymphat Res Biol. 2007;5:257-264.

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