Fibrous dysplasia in a child with mitochondrial A8344G mutation

Journal of Child Neurology

Volumn 23, Issue 12, 2008, Pages 1447-1450

  Chen, Szu Ta ^a   Fan, Pi Chuan ^a   Hwu, Wuh Liang ^a   Wu, Mei Hwan ^a  

^a NATIONAL TAIWAN UNIVERSITY HOSPITAL   (Taiwan)

Author keywords

A8344G mutation; Fibrous dysplasia; MERRF syndrome; WPW syndrome

Indexed keywords

ADENOSINE; CARNITINE; CARVEDILOL; GUANOSINE; MITOCHONDRIAL DNA; PROTEIN C FOS; UBIDECARENONE;

ARTICLE; CASE REPORT; CLINICAL FEATURE; DISEASE ASSOCIATION; DISEASE COURSE; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAPHY; ELECTROENCEPHALOGRAPHY; FAMILY HISTORY; FIBROUS DYSPLASIA; GENE MUTATION; GENE OVEREXPRESSION; GENETIC SCREENING; HEART LEFT VENTRICLE HYPERTROPHY; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; LABORATORY TEST; MALE; MERRF SYNDROME; MUTATIONAL ANALYSIS; NERVE COMPRESSION; NEUROLOGIC EXAMINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; OPTIC NERVE INJURY; OPTICAL COHERENCE TOMOGRAPHY; OSTEOBLAST; PHYSICAL EXAMINATION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SCHOOL CHILD; VISUAL DISORDER; WOLFF PARKINSON WHITE SYNDROME;

CHILD; DNA, MITOCHONDRIAL; HUMANS; MALE; MERRF SYNDROME; MITOCHONDRIAL ENCEPHALOMYOPATHIES; MUTATION;

EID: 57749205365     PISSN: 08830738     EISSN: None     Source Type: Journal    
DOI: 10.1177/0883073808318541     Document Type: Article

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