Cargando…
Freiberg’s Infarction as the First Clinical Presentation of Sneddon Syndrome
Sneddon syndrome is a rare, non-inflammatory vasculopathy that generally occurs in the third to fourth decade of life but may rarely present in the pediatric population. It is characterized by the skin finding of livedo racemosa and recurrent ischemic strokes. Other common neurologic manifestations...
Autores principales: | Samanta, Debopam, Cobb, Sarah |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7847121/ https://www.ncbi.nlm.nih.gov/pubmed/33531949 http://dx.doi.org/10.4103/jpn.JPN_159_19 |
Ejemplares similares
-
Cognitive and psychiatric changes as first clinical presentation in Sneddon syndrome
por: Fabiani, Giorgio, et al.
Publicado: (2018) -
Coexistence of scleromyxedema and Sneddon syndrome
por: Furci, Antonio, et al.
Publicado: (2021) -
Sneddon syndrome
por: Elmahi, Hakima, et al.
Publicado: (2019) -
Sneddon’s syndrome presenting with severe disabling bilateral headache
por: Cavestro, Cinzia, et al.
Publicado: (2009) -
Cognitive and psychiatric signs revealing Sneddon syndrome: A case report
por: Karoui, Mehdi, et al.
Publicado: (2023)