Characteristics of tuberous sclerosis therapy

        Tuberous sclerosis is an autosomal dominant genetic disease. Clinical symptoms with facial sebaceous tumors, epilepsy and diminished intelligence-based. More than 10 years of age before the onset of glial nodules were hyperplastic sclerosis occurred in the cerebral cortex, basal ganglia, the brain wall. Head CT showed calcification, EEG showed high amplitude loss of law and the epileptic discharge. We made of precious Tibetan medicine in the promotion of brain cell proliferation, improve brain metabolism, control of epileptic foci, improve IQ, so that children with tuberous sclerosis to continue learning and improve self-care and self-reliance.
Typical cases of tuberous sclerosis:
1, ZHANG Mei-ling Female 22 years old, Jiangsu Province, were 3-4 years old appeared peixian seizures, facial symmetry triangle nose and mouth with needles the size of the distribution of nodules. A small nodule behind the increase in puberty increases, the body had multiple Tuoshi trunk leukoplakia. Frequent seizures a month 2-3 times or 4-5 times, 2-3 minutes per episode continued, intelligence can still be. In other hospitals to do head CT showed: intracranial multiple nodules scattered to the frontal lobe, basal ganglia-based. Diagnosis of tuberous sclerosis. Adherence to treatment over the years, taking-off “more than capable, topiramate, valproate,” and many other Western and Chinese medicine was no better. Treatment of epilepsy after 6 months control, symptoms fully recovered. So far no recurrent disease, the whole family very happy.
2, Wang Yamin Female 16 years old Hunan, mental retardation, language and backward, facial sebaceous tumors, and had frequent seizures eye hair straight, confusion. Diagnosis of tuberous sclerosis. After a course of treatment of epilepsy control, intelligence, language, are significantly improved.

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