【佳學基因檢測】2型痙攣性截癱基因解碼、基因檢測

基因解碼導讀：

2型痙攣性截癱的英文表述為Spastic paraplegia type 2，是一種神經系統(tǒng)退行性變性疾病。其病理改變主要是脊髓中雙側皮質脊髓束的軸索變性和（或）脫髓鞘，以胸段最重。臨床表現(xiàn)為雙下肢肌張力增高，腱反射活躍亢進，病理反射陽性，呈剪刀步態(tài)。又稱為X連鎖隱性遺傳痙攣性截癱。

什么樣的人應當做2型痙攣性截癱基因解碼、基因檢測？

發(fā)病年齡多見于兒童期或青春期，但也可見于其他年齡段，男性略多于女性，常有遺傳家族史。臨床表現(xiàn)為緩慢進展的雙下肢痙攣性肌無力，肌張力增高，腱反射活躍亢進，膝、踝陣攣，病理征陽性，呈剪刀樣步態(tài)等。可伴有視神經萎縮、視網膜色素變性、錐體外系癥狀、小腦性共濟失調、感覺障礙、癡呆、精神發(fā)育遲滯、耳聾、肌萎縮、自主神經功能障礙等，還可有弓形足畸形。

Spastic paraplegia type 2  is part of a group of genetic disorders known as hereditary spastic paraplegias. These disorders are characterized by progressive muscle stiffness (spasticity) and the development of paralysis of the lower limbs (paraplegia). Hereditary spastic paraplegias are divided into two types: pure and complex. The pure types involve the lower limbs. The complex types involve the lower limbs and can also affect the upper limbs to a lesser degree; the structure or functioning of the brain; and the nerves connecting the brain and spinal cord to muscles and sensory cells that detect sensations such as touch, pain, heat, and sound (the peripheral nervous system). Spastic paraplegia type 2 can occur in either the pure or complex form.

People with the pure form of spastic paraplegia type 2 experience spasticity in the lower limbs, usually without any additional features. People with the complex form of spastic paraplegia type 2 have lower limb spasticity and can also experience problems with movement and balance (ataxia); involuntary movements of the eyes (nystagmus); mild intellectual disability; involuntary, rhythmic shaking (tremor); and degeneration (atrophy) of the optic nerves, which carry information from the eyes to the brain. Symptoms usually become apparent between the ages of 1 and 5 years; those affected are typically able to walk and have a normal lifespan.

2型痙攣性截癱的常規(guī)臨床檢查

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