SURF-1 gene mutation associated with leukoencephalopathy in a 2-year-old

Keyphrases

• Gene mutation 100%
• Two-year-olds 100%
• Leukoencephalopathy 100%
• Leukodystrophy 100%
• Brainstem 50%
• Deep Gray Matter 50%
• Respiratory Chain Deficiency 50%
• Leigh Syndrome 50%
• Magnetic Resonance Imaging 25%
• White Matter 25%
• Neurodegenerative 25%
• Radiological Findings 25%
• Magnetic Resonance Findings 25%
• Diffusion-weighted Imaging 25%
• Mitochondrial Disease 25%
• Diagnostic Features 25%
• White Matter Disease 25%
• Cytochrome c Oxidase Deficiency 25%
• Cytotoxic Edema 25%

Medicine and Dentistry

• Gene Mutation 100%
• Leukoencephalopathy 100%
• Leukodystrophy 100%
• Magnetic Resonance Imaging 50%
• Gray Matter 50%
• Brainstem 50%
• Respiratory Chain 50%
• Leigh's Disease 50%
• Diagnosis 25%
• Disorders of Mitochondrial Functions 25%
• Diffusion MRI 25%
• Edema 25%
• White Matter Disease 25%
• Cytochrome C Oxidase Deficiency 25%

Neuroscience

• Gene Mutation 100%
• Leukoencephalopathy 100%
• Leukodystrophy 100%
• Gray Matter 50%
• Magnetic Resonance Imaging 50%
• Brainstem 50%
• Electron Transport Chain 50%
• Leigh's Disease 50%
• Cytochrome C Oxidase 25%
• Diffusion MRI 25%
• White Matter Disease 25%
• Mitochondrial Disease 25%