Infantile encephalopathy associated with the MELAS A3243G mutation

Keyphrases

• Brain Magnetic Resonance Imaging 100%
• Mitochondrial DNA 100%
• MELAS 100%
• Infantile Encephalopathy 100%
• A3243G mutation 100%
• Seizure 66%
• Muscle Biopsy 66%
• Biopsy Specimen 66%
• Phenotypic Expression 66%
• A3243G 66%
• Ragged-red Fibers 66%
• Early Onset 33%
• Short Stature 33%
• Ataxia 33%
• Early childhood 33%
• Early Development 33%
• Neurologic Deficit 33%
• Peripheral Tissues 33%
• Neurologic 33%
• Striatal Lesion 33%
• Point mutation 33%
• Generalized Seizures 33%
• Transfer RNA (tRNA) 33%
• Early Infancy 33%
• Stroke Mimics 33%
• Childhood-onset 33%
• Lactic Acidosis 33%
• Clinical picture 33%
• Third child 33%
• Focal Neurological Deficit 33%
• Cerebral Atrophy 33%
• Cerebrospinal Fluid Lactate 33%
• Apneic Episodes 33%
• Areflexia 33%
• Atypical Features 33%
• Leigh Syndrome 33%
• Retinal pigmentary Changes 33%
• Psychomotor Delay 33%
• MELAS Syndrome 33%
• Lactate Level 33%
• Occipital Lesions 33%

Medicine and Dentistry

• Magnetic Resonance Imaging 100%
• Brain Disease 100%
• Mitochondrial DNA 100%
• Epileptic Seizure 66%
• Muscle Biopsy 66%
• Apoplexy 33%
• Short Stature 33%
• Cerebrospinal Fluid 33%
• Absence 33%
• Point Mutation 33%
• Lactic Acid 33%
• Ataxia 33%
• Lactic Acidosis 33%
• Infancy 33%
• Tonic-Clonic Seizure 33%
• Cerebral Atrophy 33%
• Leigh's Disease 33%
• Areflexia 33%
• MELAS Syndrome 33%
• Transfer RNA 33%

Neuroscience

• Encephalopathy 100%
• Magnetic Resonance Imaging 100%
• Mitochondrial DNA 100%
• Transfer RNA 33%
• Point Mutation 33%
• Epileptic Absence 33%
• Ataxia 33%
• Tonic-Clonic Seizure 33%
• Leigh's Disease 33%