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PA Consulting comments on the development and use of innovative gene therapies to treat rare diseases in an article by Joy Persaud in Raconteur’s Future of Healthcare report.
Read the full original article here
Commenting on the use of gene therapy for Retinitis Pigmentosa, PA explains: “Retinal disorders are good candidates for gene therapy,” adding “Loss of tissue in the eye is gradual, giving a wide treatment window. Nerve cells in the eye don’t divide, meaning that there is no requirement for administering further treatments. The therapy is permanent – one and done.”
PA continues, saying that one eye is treated at a time, which means the un-treated eye will note experience any adverse reactions.
Commenting on the use of gene therapy for Spinal Muscular Atrophy (SMA), PA explains that: “Patients with this disease lack the survival motor neuron protein, which is essential for the normal functioning of motor neurons. Without it, these nerve cells deteriorate and eventually die,” adding that “Diagnosis can be made via gene screening, which can be done at birth.”
Explaining the procedure, PA says: “When injected, it passes into the nerves and provides the correct gene to make enough of the protein and thereby restore nerve function.”
PA adds: “Given that there were practically no other viable permanent treatment options available before, the significance of Zolgensma’s introduction as a treatment for SMA should not be underestimated.”