First TSD is an inherited condition and the early symptoms of the disease among infants appear at the age of six months when a healthy child abruptly stops “smiling, crawling or turning over, loses the ability to grasp or reach out, and in a gradual way becomes blind and paralyzed†(USA TODAY, N.d). The disease cannot be transmitted since it is only acquired through hereditary means, and there is no possibility of it occurring in the future unless one is born with it.
Currently, there exists no treatment for TSD, which can be used to prevent the disease, and most programs in place largely address the ways of making infected children more comfortable (USA TODAY, N.d). Some of the treatment options with regard to this include “respiratory care, assistive devices, medication, physical therapy, support for the family, coordination with primary care physician†(MAYO CLINIC, N.d).
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