Utility of Whole Blood Thiamine Pyrophosphate Evaluation in TPK1-Related Diseases

TPK1 mutations are a rare, but potentially treatable, cause of thiamine deficiency. Diagnosis is challenging given the phenotypic overlap that exists with other metabolic and neurological disorders. We report a case of TPK1-related disease presenting with Leigh-like syndrome and review the diagnosti...

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Detalles Bibliográficos
Autores principales: Bugiardini, Enrico, Pope, Simon, Feichtinger, René G., Poole, Olivia V., Pittman, Alan M., Woodward, Cathy E., Heales, Simon, Quinlivan, Rosaline, Houlden, Henry, Mayr, Johannes A., Hanna, Michael G., Pitceathly, Robert D.S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6679130/
https://www.ncbi.nlm.nih.gov/pubmed/31288420
http://dx.doi.org/10.3390/jcm8070991

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6679130/
https://www.ncbi.nlm.nih.gov/pubmed/31288420
http://dx.doi.org/10.3390/jcm8070991

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