Comprehensive diagnostics in a case of hereditary diffuse leukodystrophy with spheroids

BACKGROUND: Hereditary diffuse leukodystrophy with spheroids is a rare type of leukoencephalopathy. Mutations in the colony stimulating factor 1 receptor have recently been identified to be the cause of this microgliopathy. Clinical and radiological presentation can often misguide physicians during...

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Detalles Bibliográficos
Autores principales: Meyer-Ohlendorf, Marie, Braczynski, Anne, Al-Qaisi, Omar, Gessler, Florian, Biskup, Saskia, Weise, Lutz, Steinbach, Joachim P., Wagner, Marlies, Mittelbronn, Michel, Bähr, Oliver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4491230/
https://www.ncbi.nlm.nih.gov/pubmed/26141177
http://dx.doi.org/10.1186/s12883-015-0368-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4491230/
https://www.ncbi.nlm.nih.gov/pubmed/26141177
http://dx.doi.org/10.1186/s12883-015-0368-3

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