DOI: 10.14704/nq.2016.14.2.947

Integrated Quantum Therapy in an Epileptic Child after 13 Years of Inherited Real Risk of Epilepsy in Evolution: A Case Study

Marco Marchionni, Simone Caramel, Sergio Stagnaro

Abstract


The comprehension of the pathogenesis of epilepsy finds a new impulse in studies on non-linear dynamics of EEG signals and in the growing genetic molecular evidence of the mitochondrial origin of this disease. These data are consistent with the information known by Quantum Biophysical Semeiotics that clinically investigates microcirculation both on a functional (i.e. by studying its non-linear dynamics), and on a structural viewpoint. Microcirculatory dysfunctions reflect those of a genetically altered mit-DNA and of a functional mitochondrial cytopathy known as Congenital Acidosic Enzyme-Metabolic Histangiopathy, originating from this mutation and which is particularly intense both in patients with epilepsy and in those with Inherited Real Risk of epilepsy. Preclinical diagnosis of Inherited Real Risk of epilepsy presents the opportunity to examine subjects with a predisposition to this disease since birth in order to perform an efficient pre-primary and primary prevention. In our case report, an integrated quantum therapy applied to a child with Inherited Real Risk of epilepsy in strong evolution provides encouraging satisfactory results.

Keywords


epilepsy diagnosis; mitochondrial dysfunction; primary prevention; quantum therapy; deterministic chaos

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References


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Supporting Agencies

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.



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