Hereditary spastic paraplegia 51

Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the AP4E1 gene.

Also known as: AP4E1 hereditary spastic paraplegia, SPG51, Spastic Paraplegia 51, hereditary spastic paraplegia caused by mutation in AP4E1, hereditary spastic paraplegia type 51, cerebral palsy, spastic quadriplegic, 4, cerebral palsy, spastic quadriplegic, 4, formerly, spastic paraplegia 51, autosomal recessive

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