This page lists all known medications that could potentially lead to 'Spastic paralysis' as a side effect. It's important to note that mild side effects are quite common with medications. The ...
Patients with spastic paraplegia type 15 develop movement disorders during adolescence that may ultimately require the use of a wheelchair. In the early stages of this rare hereditary disease the ...
Since she was born 20 years ago, Sylva Eugenie Davis of Kansas City has not been able to use her arms or legs. The nerve tracts in the neck region of her spinal cord were injured at birth, causing ...
Mutations in 3 genes (SPG4, SPG3, and SPG31) are implicated in one half of the autosomal dominant hereditary spastic paraplegias, which are part of the larger group of hereditary spastic diplegias ...
Hereditary spastic paraplegia (HSP), also known as familial spastic paraparesis, is a term used for a group of inherited diseases that affect the upper motor neurons traveling from the brain through ...
A joint study conducted by the University of Bonn and the DZNE has confirmed early-stage brain inflammation in mice. Patients with spastic paraplegia type 15 develop movement disorders during ...
Spastic paraplegia (SP) in hereditary form is a genetically and clinically heterogeneous group of diseases with distinctive features of axonal degeneration in corticospinal tracts. Progressive ...
Hereditary spastic paraplegia (HSP) comprises a heterogeneous group of neurodegenerative disorders that are mainly characterised by progressive spasticity and weakness of the lower limbs. Recent ...
Newark, New Castle, USA, April 13, 2023 (GLOBE NEWSWIRE) -- The global hereditary spastic paraplegia market is projected to register a revenue CAGR of 6.70%, according to the latest evaluation by ...
Patients with spastic paraplegia type 15 develop movement disorders during adolescence that may ultimately require the use of a wheelchair. In the early stages of this rare hereditary disease, the ...
Hereditary spastic paraplegias refers to a clinically and genetically heterogenous disorders that are characterised by lower extremity spasticity and weakness. When the symptoms of this disease behind ...