Oculoleptomeningeal Amyloidosis associated with transthyretin Leu12Pro in an African patient

Oculoleptomeningeal amyloidosis is a rare manifestation of hereditary transthyretin (TTR) amyloidosis. Here, we present the first case of leptomeningeal amyloidosis associated with the TTR variant Leu12Pro mutation in an African patient. A 43-year-old right-handed Nigerian man was referred to our ce...

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Detalles Bibliográficos
Autores principales: McColgan, P., Viegas, S., Gandhi, S., Bull, K., Tudor, R., Sheikh, F., Pinney, J., Fontana, M., Rowczenio, D., Gillmore, J. D., Gilbertson, J. A., Whelan, C. J., Shah, S., Jaunmuktane, Z., Holton, J. L., Schott, J. M., Werring, D. J., Hawkins, P. N., Reilly, M. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2014
Materias:
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4289971/
https://www.ncbi.nlm.nih.gov/pubmed/25488473
http://dx.doi.org/10.1007/s00415-014-7594-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4289971/
https://www.ncbi.nlm.nih.gov/pubmed/25488473
http://dx.doi.org/10.1007/s00415-014-7594-2

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