Familial ALS with SOD1 mutation misdiagnosed with polyradiculopathy and myopathy

Keyphrases

• Myopathy 100%
• Familial ALS 100%
• Polyradiculopathy 100%
• Superoxidase Dismutase 100%
• Gene mutation 50%
• Young Males 50%
• Muscle Biopsy 50%
• Laminectomy 50%
• Lumbosacral 50%
• Denervation 50%
• Amyotrophic Lateral Sclerosis 50%
• Respiratory muscle Strength 50%
• Upper Motor Neuron Signs 50%
• Cu-Zn 50%
• Lower Extremity Weakness 50%
• Spinal Stenosis 50%
• Chronic Denervation 50%
• CK Elevation 50%

Neuroscience

• Muscle Disorder 100%
• Amyotrophic Lateral Sclerosis 100%
• Denervation 66%
• Gene Mutation 33%
• Upper Motor Neuron 33%
• Spinal Stenosis 33%