Hereditary spastic paraplegia
(Redirected from Kjellin syndrome)
Hereditary Spastic Paraplegia (HSP) is a group of inherited disorders that are characterized by progressive weakness and stiffness of the legs.
Symptoms[edit | edit source]
The primary symptom of HSP is progressive spasticity in the lower limbs, due to degeneration of the nerves that control muscle movement. Other symptoms can include general weakness, muscle spasms, and difficulties with balance and coordination. Some forms of HSP can also affect the upper body, causing symptoms such as numbness, tingling, or pain in the arms and hands.
Causes[edit | edit source]
HSP is caused by mutations in various genes. The different types of HSP are classified according to the genetic cause. The most common types of HSP are caused by mutations in the SPG4, SPG3A, and SPG31 genes.
Diagnosis[edit | edit source]
Diagnosis of HSP is based on the presence of characteristic clinical features and a family history of the disorder. Genetic testing can confirm the diagnosis in some cases.
Treatment[edit | edit source]
There is currently no cure for HSP, but treatment can help to manage symptoms. This can include physical therapy, occupational therapy, and medication to manage spasticity and other symptoms.
See also[edit | edit source]
| Hereditary spastic paraplegia Resources | |
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