Sneddon's syndrome

Ecaterina Bontas, Akiko Tanikawa, Andreea Cristina Mitu, Cornelia Predescu, Daniela Bartos, Semona Vizeteu, Maria Dorobanţu

研究成果: Review article査読

抄録

Sneddon's syndrome is a rare non-inflammatory arteriopathy labeled as a neurodermatologic disorder and defined by multiple cerebrovascular accidents and extensive livedo racemosa. It is a slowly progressive condition, and often unrecognized. The condition has a slow progress starting with non - specific symptoms, then livedo racemosa, and later, neurological involvement Autoimmune process against the endothelial cell has been observed, particularly occurring in combination with the Hughes antiphospholipid antibody syndrome The diagnosis of Sneddon's syndrome needs extensive laboratory evaluation. There is no specific investigation in Sneddon's syndrome, and the only diagnostic criterion is the histological exam of skin biopsy. There is no specific treatment for Sneddon's syndrome, only the symptomatic and supportive measures.

本文言語English
ページ(範囲)219-222
ページ数4
ジャーナルArchives of the Balkan Medical Union
41
4
出版ステータスPublished - 2006 12

ASJC Scopus subject areas

  • 医学(全般)

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