Autosomal dominant spastic paraplegia type 17 (SPG17) is a rare, inherited neurological disorder characterized by progressive spasticity (stiffness) and weakness of the legs. It is caused by mutations in the SPG17 gene, which is located on chromos...

Autosomal dominant spastic paraplegia type 19 (SPG19) is a rare, inherited neurological disorder characterized by progressive spasticity (stiffness) and weakness of the legs. It is caused by mutations in the SPG19 gene, which is located on chromos...

Autosomal dominant spastic paraplegia type 29 (SPG29) is a rare, inherited neurological disorder characterized by progressive spasticity (stiffness) and weakness of the legs. It is caused by mutations in the SPG29 gene, which is located on chromos...

Autosomal dominant spastic paraplegia type 3 (SPG3) is a rare, inherited neurological disorder characterized by progressive spasticity (stiffness) and weakness of the lower limbs. It is caused by mutations in the SPG3A gene, which is located on ch...

Autosomal dominant spastic paraplegia type 31 (SPG31) is a rare, inherited neurological disorder characterized by progressive spasticity (stiffness and tightness of the muscles) and weakness of the lower limbs. It is caused by mutations in the SPG...

Autosomal dominant spastic paraplegia type 36 (SPG36) is a rare, inherited neurological disorder characterized by progressive spasticity (stiffness and difficulty with movement) of the lower limbs. It is caused by mutations in the SPG36 gene, whic...

Autosomal dominant spastic paraplegia type 37 (SPG37) is a rare, inherited neurological disorder characterized by progressive spasticity (stiffness) and weakness of the legs. It is caused by mutations in the SPG37 gene, which is located on chromos...

Autosomal dominant spastic paraplegia type 38 (SPG38) is a rare, inherited neurological disorder characterized by progressive spasticity (stiffness and difficulty with movement) of the lower limbs. It is caused by mutations in the KIF5A gene, whic...

Autosomal dominant spastic paraplegia type 4 (SPG4) is a rare, inherited neurological disorder characterized by progressive muscle stiffness and weakness in the legs (spasticity) and difficulty walking (paraplegia). It is caused by mutations in th...

Autosomal dominant spastic paraplegia type 41 (SPG41) is a rare, inherited neurological disorder characterized by progressive spasticity (stiffness and difficulty with movement) of the lower limbs. It is caused by mutations in the SPG41 gene, whic...

Autosomal dominant spastic paraplegia type 42 (SPG42) is a rare, inherited neurological disorder characterized by progressive spasticity (stiffness) and weakness of the lower limbs. It is caused by mutations in the SPG42 gene, which is located on ...

Autosomal dominant spastic paraplegia type 6 (SPG6) is a rare, inherited neurological disorder characterized by progressive spasticity (stiffness) and weakness of the lower limbs. It is caused by mutations in the SPG6 gene, which is located on chr...

Autosomal dominant spastic paraplegia type 73 (SPG73) is a rare, inherited neurological disorder characterized by progressive spasticity (stiffness) and weakness of the legs. It is caused by mutations in the SPG73 gene, which is located on chromos...

Autosomal dominant spastic paraplegia type 8 (SPG8) is a rare, inherited neurological disorder characterized by progressive spasticity (stiffness) and weakness of the legs. It is caused by mutations in the KIF5A gene, which is responsible for the ...

Autosomal dominant spastic paraplegia type 9A (SPG9A) is a rare, inherited neurological disorder characterized by progressive spasticity (stiffness) and weakness of the legs. It is caused by mutations in the KIF5A gene, which is responsible for th...

Autosomal dominant spastic paraplegia type 9B (SPG9B) is a rare, inherited neurological disorder characterized by progressive spasticity (stiffness) and weakness of the legs. It is caused by mutations in the KIF5A gene, which is responsible for th...