Hereditary spastic paraplegia associated with axonal neuropathy: A novel mutation of SPG3A in a large family

Medicine and Dentistry

• DeJerine-Sottas Disease 100%
• Neuropathy 100%
• Spastic Paraplegia 100%
• Surveillance 50%
• Follow up 50%
• Autosomal Dominant Inheritance 50%
• Patient Population 50%
• Neurological Complication 50%

Neuroscience

• Hereditary Spastic Paraplegia 66%
• Paraplegia 66%

Agricultural and Biological Sciences

• Mutation 100%