The outbreak of Guillain-Barré Syndrome (GBS) in Pune and the ninth death due to the disease in the city have surprised the doctors. An unusually rapid disease progression is being reported in ...

Experts told TOI that Pune's higher mortality and severe disease progression indicated predominance of Acute Motor Axonal Neuropathy (AMAN) variant, a more aggressive form of GBS associated with ...

This is a diffuse motor-sensory polyneuropathy that is predominantly axonal in nature. The neuropathy is present regardless of the etiology of the cirrhosis. The incidence and severity of this ...

acute motor axonal neuropathy (AMAN) and acute motor and sensory axonal neuropathy (AMSAN). The clinical course was found to be no different from that of non-HIV cases ( Table 9). Three patients ...

The other types include Acute Motor Axonal Neuropathy (AMAN) and Acute Motor Sensory Axonal Neuropathy (AMSAN). "Some patients complain of tinnitus, muscle weakness, gait disturbances, tachycardia ...

Low levels of NfL are released continuously under normal conditions, but a significant increase can occur in response to axonal damage ... which causes motor neuron degeneration.

PUNE: The ninth casualty linked to Guillain-Barre Syndrome in Pune, a 34-year-old resident of Wagholi, showed symptoms that surprised his doctors. The patient had complained of loose motions for ...

Find Neuropathy Axon stock video, 4K footage, and other HD footage from iStock. Get higher quality Neuropathy Axon content, for less—All of our 4K video clips are the same price as HD. Video Back ...

Quadriparesis is when there is muscle weakness in both arms and both legs. It is different than quadriplegia, which causes paralysis (complete loss of movement) in each of the body’s limbs. The ...

A decision was made for the patient to undergo extensive genetic testing to probe the cause of his severe neuropathy ... involving demyelination of both the motor and sensory nerves; this was ...

Nerve conduction studies show a demyelinating peripheral neuropathy ... and rapid motor decline. Most patients are fully dependent within 5 years of symptom onset. In one case, pathological features ...