New drug research raises hope for Rett syndrome treatment
Rett Syndrome is a commonly
found cause for the genetic conditions in women which lead to intellectual
disability. It affects the development of the brain which resulting in
progressive inability to use muscles for body movements, eye while developing
speaking disabilities. Studies suggest the syndrome is frequently suspected in
girls.
Presently, there’s no treatment available that can manage the
symptoms or the epileptic and respiratory problems faced in by the Rett
syndrome patients. There are a couple of research projects which are partially funded
by EU.
Recent research on the Rett syndrome market studies if a
drug that inhibits a central neuroinflammatory protein (GSK3B) could reverse
part of the symptoms. The preclinical model of the disease has been initiated
in the research which is conducted in mice since they have the same deficiency
of protein 2 as found in human Rett syndrome.
Global Rett syndrome market research suggests such variant forms of the condition occur due to
the mutations in the MECP2 gene. This gene offers instructions for making a
protein required for the normal brain to function.
As per the market research reports on the Rett Syndrome, the
results of this healthcare research project are expected to be promising.
The SB216763 agent contributed to reducing tremors and breathing
difficulties in animals while also dealing with the movability limitations.
The sleeping neurons of the
syndrome get awaked with the inhibition of GSK3B agents and the brain cells
begin to recover their contact between them. This further increases the
communication between the neuronal synapses and liven up the brain cells to
function normally.
The latest healthcare market research reports have provided a new method
to better the quality of life of Rett syndrome patients. The applicability in
patients is soon to be started helping them recover from the disability.
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