Long-term tracking of neurological complications of encephalopathy and myopathy in a patient with nephropathic cystinosis: a case report and review of the literature

INTRODUCTION: Cystinosis is a hereditary storage disease resulting in intracellular accumulation of cystine and crystal formation that causes deterioration of the function of many organs. The major clinical symptom is renal failure, which progresses and necessitates renal transplantation at the begi...

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Detalles Bibliográficos
Autores principales: Müller, Marcus, Baumeier, Andrea, Ringelstein, EB, Husstedt, IW
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2491650/
https://www.ncbi.nlm.nih.gov/pubmed/18644104
http://dx.doi.org/10.1186/1752-1947-2-235

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2491650/
https://www.ncbi.nlm.nih.gov/pubmed/18644104
http://dx.doi.org/10.1186/1752-1947-2-235

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