Leigh disease with mitochondrial DNA A8344G mutation: case report and brief review.

Tsao, Chang-Yong; Herman, Gail; Boué, Daniel R; Prior, Thomas W; Lo, Warren D; Atkin, Joan F; Rusin, Jerome

Tsao, Chang-Yong; Herman, Gail; Boué, Daniel R; Prior, Thomas W; Lo, Warren D; Atkin, Joan F; Rusin, Jerome.

Affiliation

Tsao CY; Department of Pediatrics, The Ohio State University, Children's Radiological Institute, Children's Hospital, Columbus, USA. ctsao@chi.osu.edu

J Child Neurol ; 18(1): 62-4, 2003 Jan.

Article in En | MEDLINE | ID: mdl-12661941

Subject(s)

DNA Mutational Analysis; DNA, Mitochondrial/genetics; Intellectual Disability/genetics; Leigh Disease/genetics; Point Mutation/genetics; Brain/pathology; Humans; Infant; Intellectual Disability/diagnosis; Leigh Disease/diagnosis; Magnetic Resonance Imaging; Male; Neurologic Examination; Phenotype

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Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / DNA Mutational Analysis / Leigh Disease / Point Mutation / Intellectual Disability Type of study: Diagnostic_studies Limits: Humans / Infant / Male Language: En Journal: J Child Neurol Journal subject: NEUROLOGIA / PEDIATRIA Year: 2003 Document type: Article Affiliation country: United States Country of publication: United States

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