电邮这篇文章 TUBEROUS SCLEROSIS
- 作者: Vazhbin L.B1, Belova N.I1, Ltezvinskaya E.M1, Stribuk P.V1
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隶属关系:
- 期: 卷 16, 编号 1 (2013)
- 页面: 6-9
- 栏目: Articles
- URL: https://rjsvd.com/1560-9588/article/view/36735
- DOI: https://doi.org/10.17816/dv36735
- ID: 36735
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A case with a rare hereditary disease — tuberous sclerosis - is described. In addition to skin involvement, the disease is characterized by congenital epidermal dysplasia involvement of the nervous system, organ of vision, cardiovascular system, kidneys, and other organs and systems. The authors emphasize the importance of complete examinations of these patients with consideration for the probable visceral involvement.
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参考
- Дорофеева М.Ю. Туберозный склероз у детей. Российский вестник перинатологии и педиатрии. 2001; 4: 33—41.
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- Вульф К., Джонсон Р., Сюрмон Д. Дерматология по Томасу Фитцпатрику. М.: Практика; 2007. 2.
- Osbone I.P., Fruer A., Webb D. Epidemiology of tuberous sclerosis. Ann. N. Y. Acad. Sci. 1991; 615: 125—8.
- Hoffman Ch., Schreiner W.D. Residivierender Spontanpneumothtomorax Symptom des Morbus Bourneville—Pringle. Hautarzt. 1980; 31(2): 91—5.
- Hunt A. Psychiatric and Psychological Aspects. In: Gomes M., Sampson J., Whittemore V., eds. Tuberous sclerosis. New York-Oxford: Oxford University Press; 1999: 47—62.
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