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infantile-onset ascending spastic paralysis
Genetics:
- associated with mutations in the gene for alsin
Clinical manifestations:
- progressive spasticity & weakness of limbs
Related
alsin; amyotrophic lateral sclerosis 2 chromosomal region candidate gene 6 protein; amyotrophic lateral sclerosis 2 protein (ALS2 ALS2CR6 KIAA1563)
General
genetic disease of the central nervous system
motor neuron disease
Database Correlations
OMIM 607225
References
OMIM :accession 607225