Thiamine pyrophosphokinase deficiency causes a Leigh Disease like phenotype in a sibling pair: identification through whole exome sequencing and management strategies

We present a sibling pair with Leigh-like disease, progressive hypotonia, regression, and chronic encephalopathy. Whole exome sequencing in the younger sibling demonstrated a homozygous thiamine pyrophosphokinase (TPK) mutation. Initiation of high dose thiamine, niacin, biotin, α-lipoic acid and ket...

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Detalles Bibliográficos
Autores principales: Fraser, Jamie L., Vanderver, Adeline, Yang, Sandra, Chang, Taeun, Cramp, Laura, Vezina, Gilbert, Lichter-Konecki, Uta, Cusmano-Ozog, Kristina P., Smpokou, Patroula, Chapman, Kimberly A., Zand, Dina J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5121315/
https://www.ncbi.nlm.nih.gov/pubmed/27896076
http://dx.doi.org/10.1016/j.ymgmr.2013.12.007

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5121315/
https://www.ncbi.nlm.nih.gov/pubmed/27896076
http://dx.doi.org/10.1016/j.ymgmr.2013.12.007

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