A rare mitochondrial disorder: Leigh sydrome - a case report

Leigh syndrome is a rare progressive neurodegenerative, mitochondrial disorder of childhood with only a few cases documented from India. The clinical presentation of Leigh syndrome is highly variable. However, in most cases it presents as a progressive neurological disease with motor and intellectua...

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Detalles Bibliográficos
Autores principales: Shrikhande, Dhananjay Y, Kalakoti, Piyush, Syed, MM Aarif, Ahya, Kunal, Singh, Gurmeet
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2949674/
https://www.ncbi.nlm.nih.gov/pubmed/20843336
http://dx.doi.org/10.1186/1824-7288-36-62

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2949674/
https://www.ncbi.nlm.nih.gov/pubmed/20843336
http://dx.doi.org/10.1186/1824-7288-36-62

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