10 top medical experts on Autosomal Dominant Spastic Paraplegia 42 across 2 countries, including 1 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Autosomal Dominant Spastic Paraplegia 42: A pure form of hereditary spastic paraplegia characterized by slowly progressive spastic paraplegia of lower extremities with an age of onset ranging from childhood to adulthood and patients presenting with spastic gait, increased tendon reflexes in lower limbs, extensor plantar response, weakness and atrophy of lower limb muscles and, in rare cases, pes cavus. No abnormalities are noted on magnetic resonance imaging.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
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