What Is Publish Polio Syndrome? Know All About It newsfragment


Polio happens because of polio virus which is one of those enterovirus and there’s any other time period for polio which we name paralytic polio. It happens round 0.5 to 0.05% of the infectious people and reasons sickness of the anterior horn cells of the spinal wire. Consistent with Dr. Puja Kushwah, who’s a Sr. Guide of Neurology, at Metro Medical institution, Noida, “Due to their damage, the patient gets paralytic polio whose symptoms vary greatly depending on the condition of the legs. Paralysis is more commonly seen in the legs as compared to the upper limbs. There is a term in polio which we call post polio syndrome where in a patient who has had paralytic polio, starts feeling more weak after around 15 years.”

Unmasking The Unrevealed Ache: Figuring out Publish-Polio Syndrome

Dr. Siddhant Mahajan- who’s the Founding father of StemRX Nutraceuticals mentioned, “Post-polio syndrome (PPS), a condition that can emerge decades after the initial infection, continues to affect millions of people worldwide. It is a condition that typically strikes polio survivors 15 to 40 years after their initial recovery. The precise cause of PPS remains elusive, but experts believe it may be related to the excessive stress that polio places on motor neurons. Over time, these overworked neurons may start to deteriorate, leading to the characteristic symptoms of PPS.”

“Symptoms of PPS can vary widely among individuals but commonly include muscle weakness, fatigue, muscle and joint pain, and difficulties with breathing or swallowing. Many PPS patients also report a heightened sensitivity to cold temperatures, which can exacerbate their symptoms. These physical challenges can result in a significantly reduced quality of life, as patients struggle with daily activities that were once manageable. Due to nerve involvement and infection, the patient develops lower limb weakness with foot drop and muscular atrophy of the lower limb,” he added.

The Street Forward: Regenerative Drugs’s Agreement

Generation there’s no medication for Publish-Polio Syndrome, researchers are increasingly more turning to regenerative drugs as a possible supply of hope for sufferers affected by this debilitating situation. Dr. Siddhant Mahajan mentioned that regenerative drugs harnesses the frame’s personal skill to fix and regenerate broken tissues, providing a booklet strategy to treating a large area of illnesses and accidents.

“One promising avenue in regenerative medicine for PPS involves mesenchymal cell therapy. These cells have the unique ability to differentiate into various cell types, making them a potential solution for replenishing the damaged motor neurons in PPS patients. By introducing healthy mesenchymal cells into the affected areas, researchers hope to stimulate the regeneration of damaged neurons, thereby improving muscle function and reducing pain,” he persisted to mention.

“Additionally, advances in regenerative medicine have led to the development of innovative therapies like tissue engineering and gene therapy, which hold immense potential in treating PPS. Tissue engineering can create artificial muscle tissues that could potentially replace damaged muscle, while gene therapy aims to correct the underlying genetic and molecular factors contributing to PPS,” he added.

Publish Polio Syndrome Highlighting Ocular Motion:

On this regard, Dr Ananya Ganguly, who’s a Guide of paediatric and Complete Ophthalmology Services and products, at Disha Ocular Hospitals mentioned, “Though poliomyelitis is contagious, PPS is not. Only a polio survivor may or may not develop post polio syndrome or PPS. PPS is a result of progressive deterioration of motor neurons which leads to loss of muscle strength and dysfunction. Now this musculoskeletal weakness may also present in the form of abnormal eye movements. Over 10 percent of patients with bulbar polio have cranial nerve involvement that affects eyes or orbital musculature or both in the form  of extra ocular muscle palsy, posits, pupillary disturbance or total ophthalmologist. Definitive diagnosis of PPS still remains in the domain of research, however tests like Electromyography, MRI form useful supportive tools for the same. Lastly, as with all PPS, other causes of eye movement abnormalities must be ruled out first. Any abnormal  eye movement must be evaluated without delay since they may be symptoms of an underlying neurological disease requiring urgent management.”

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