Contents

Search


primary juvenile lateral sclerosis

closely related to but clinically distinct from amyotrophic lateral sclerosis. Epidemiology: rare Pathology: - progressive paralytic disorder resulting from upper motor neuron disease with lower motor neurons unaffected Genetics: - associated with mutations in the gene for alsin

Related

alsin; amyotrophic lateral sclerosis 2 chromosomal region candidate gene 6 protein; amyotrophic lateral sclerosis 2 protein (ALS2 ALS2CR6 KIAA1563)

General

amyotrophic lateral sclerosis (ALS); Lou Gerig's disease genetic disease of the central nervous system

Database Correlations

OMIM 606353

References

OMIM :accession 606353