Conditions / Genetic
amyotrophic lateral sclerosis type 26
info · Genetic
An amyotrophic lateral sclerosis that is characterized by adult onset of upper and low motor neuron disease causing bulbar dysfunction and limb weakness and that has_material_basis_in heterozygous mutation in the TIA1 gene on chromosome 2p13.
Signs and symptoms
- Lewy bodies
- Amyotrophic lateral sclerosis
- Frontotemporal dementia
- Bulbar palsy
- Aphasia
- Limb muscle weakness
- Memory impairment
- Personality changes