Hereditary spastic paraplegia 52

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the AP4S1 gene.

Also known as: AP4S1 hereditary spastic paraplegia, SPG52, Spastic Paraplegia 52, hereditary spastic paraplegia 52, hereditary spastic paraplegia caused by mutation in AP4S1, hereditary spastic paraplegia type 52, cerebral palsy, spastic quadriplegic, 6, cerebral palsy, spastic quadriplegic, 6, formerly

1 clinical trial for this condition and its sub-types.