Autosomal recessive spastic paraplegia type 39 (SPG39) is a rare, inherited neurological disorder characterized by progressive muscle weakness and stiffness (spasticity) in the legs. It is caused by mutations in the SLC33A1 gene, which is responsi...

Autosomal recessive spastic paraplegia type 43 (SPG43) is a rare, inherited neurological disorder characterized by progressive muscle weakness and stiffness (spasticity) in the legs. It is caused by mutations in the KIF5A gene, which is responsibl...

Autosomal recessive spastic paraplegia type 44 (SPG44) is a rare, inherited neurological disorder characterized by progressive muscle weakness and stiffness (spasticity) in the legs. It is caused by mutations in the SLC33A1 gene, which is responsi...

Autosomal recessive spastic paraplegia type 45 (SPG45) is a rare, inherited neurological disorder characterized by progressive muscle weakness and stiffness (spasticity) in the legs. It is caused by mutations in the SPG45 gene, which is located on...

Autosomal recessive spastic paraplegia type 46 (SPG46) is a rare, inherited neurological disorder characterized by progressive muscle weakness and stiffness (spasticity) in the legs. It is caused by mutations in the SLC33A1 gene, which is responsi...

Autosomal recessive spastic paraplegia type 48 (SPG48) is a rare, inherited neurological disorder characterized by progressive muscle weakness and stiffness (spasticity) in the legs. It is caused by mutations in the SLC33A1 gene, which is responsi...

Autosomal recessive spastic paraplegia type 53 (SPG53) is a rare, inherited neurological disorder characterized by progressive muscle weakness and stiffness (spasticity) in the legs. It is caused by mutations in the KIF5A gene, which is involved i...

Autosomal recessive spastic paraplegia type 54 (SPG54) is a rare, inherited neurological disorder characterized by progressive muscle weakness and stiffness (spasticity) in the legs. It is caused by mutations in the KIF5A gene, which is involved i...

Autosomal recessive spastic paraplegia type 55 (SPG55) is a rare, inherited neurological disorder characterized by progressive muscle weakness and stiffness (spasticity) in the legs. It is caused by mutations in the KIF5A gene, which is responsibl...

Autosomal recessive spastic paraplegia type 56 (SPG56) is a rare, inherited neurological disorder characterized by progressive muscle weakness and stiffness (spasticity) in the legs. It is caused by mutations in the KIF5A gene, which is involved i...

Autosomal recessive spastic paraplegia type 57 (SPG57) is a rare, inherited neurological disorder characterized by progressive muscle weakness and stiffness (spasticity) in the legs. It is caused by mutations in the KIF5A gene, which is responsibl...

Autosomal recessive spastic paraplegia type 59 (SPG59) is a rare, inherited neurological disorder characterized by progressive muscle weakness and stiffness (spasticity) in the legs. It is caused by mutations in the KIF5A gene, which is involved i...

Autosomal recessive spastic paraplegia type 5A (SPG5A) is a rare, inherited neurological disorder characterized by progressive muscle weakness and stiffness (spasticity) in the legs. It is caused by mutations in the SPG5 gene, which is responsible...

Autosomal recessive spastic paraplegia type 60 (SPG60) is a rare, inherited neurological disorder characterized by progressive muscle weakness and stiffness (spasticity) in the legs. It is caused by mutations in the KIF5A gene, which is responsibl...

Autosomal recessive spastic paraplegia type 61 (SPG61) is a rare, inherited neurological disorder characterized by progressive muscle weakness and stiffness (spasticity) in the legs. It is caused by mutations in the KIF5A gene, which is involved i...

Autosomal recessive spastic paraplegia type 62 (SPG62) is a rare, inherited neurological disorder characterized by progressive muscle weakness and stiffness (spasticity) in the legs. It is caused by mutations in the SLC33A1 gene, which is responsi...

Autosomal recessive spastic paraplegia type 63 (SPG63) is a rare, inherited neurological disorder characterized by progressive muscle weakness and stiffness (spasticity) in the legs. It is caused by mutations in the SLC12A6 gene, which is involved...