Hereditary spastic paraplegia 48 is an inherited neurological condition characterized predominantly by slowly progressive spasticity of the lower limb...

Hereditary spastic paraplegia 49 is a very rare neurodevelopmental condition caused by mutations in the TECPR2 gene. It primarily affects motor functi...

Hereditary spastic paraplegia 50 is a neurodevelopmental condition caused by pathogenic variants in the AP4M1 gene. It primarily affects motor functio...

Hereditary spastic paraplegia 52 is a neurological condition that primarily affects motor function and intellectual ability, caused by mutations in th...

Hereditary spastic paraplegia 54 is a rare, complex neurological condition that primarily affects motor function, with early childhood onset of progre...

Hereditary spastic paraplegia 5A is a neurological condition that primarily affects the motor pathways controlling the lower limbs. It manifests as a...

Hereditary spastic paraplegia 61 is a rare, complex condition that primarily affects motor function, with symptoms becoming apparent in infancy. Child...

Hereditary spastic paraplegia 7 is a condition that primarily affects motor function through progressive lower limb weakness and spasticity. It is ass...