Troyer syndrome 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).
Prognosis varies, although the disease is progressive. Some patients may have a mild form of the disease while others eventually lose the ability to walk normally. Troyer syndrome does not shorten the normal life span.
PROGNOSIS
Troyer syndrome is relentlessly progressive. Speech often becomes nearly unintelligible and locomotion impossible in the fourth to fifth decades of life. There may be some dysphagia late in life but none have required percutaneous enterogastostomy.
Treatment
Treatment
Cap Anti Troyer (1 Cap TDS )
Syp Anti Troyer (1 Teasponful TDS)
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