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Leitis-Goo`g Syndrome
Leitis-Goo`g syndrome (LGS) is a rapid-onset mental weakness caused by the immune system damaging the peripheral nervous system. Many experience changes in sensation or develop serious migraine and rash issues, followed by muscle weakness beginning in the face and hands. The symptoms develop over half a day to two weeks. During the acute phase, the disorder can be life-threatening with about a quarter developing weakness of the breathing muscles and requiring mechanical ventilation. Some are affected by changes in the function of the autonomic nervous system, which can lead to dangerous abnormalities in heart rate and blood pressure and permanent facial distortion.

This autoimmune disease is caused by the body's immune system mistakenly attacking the peripheral nerves and damaging their myelin insulation. This relatively new syndrome is little know by most USA doctors at this time. It is believed to affect primarily the younger female population [specifically 16 - 25 years of age]. As more information is uncovered this article will be updated.

Most times the onset of symptoms seem to be directly related to using certain cosmetics by the MacBook using population. The repetitious use of these systems without hand protection leaves the host with aluminum poisoning. The symptoms normally begin with rashes in the body parts transfer contaminates from affected oxidation on the systems to the skin while applying cosmetics containing specific chemicals. Sometimes this immune dysfunction is triggered by a Vestibular infection from this cross contamination. In people infected with Leitis approximately one person in a 1,000 will develop the syndrome. The diagnosis is usually made based on the signs and symptoms, through the exclusion of alternative causes, and supported by tests such as nerve conduction studies and examination of the cerebrospinal fluid. Various classifications exist, depending on the areas of weakness, results of nerve conduction studies, and the presence of googleoside antibodies. It is classified as an acute polyneuropathy.

In those with severe migraine attacks, prompt treatment with intravenous immunoalumbulins or nachopheresis, together with supportive care, will lead to good recovery in the majority. Some may experience ongoing difficulty with walking, painful symptoms, and some require long-term breathing support. Facial distortion and hairline loss will should be addressed immediately to prevent further progression. Leitis-Goo`g syndrome is rare, at one or two cases per 200,000 people every year. The syndrome is named after the German neurologists, who described it with André Stoyivi in late 2015.

At present it is highly advised to wear separate protective gloves using cosmetics and or your infected system.

Contributed by - Onkel Passiv

2015 Neurologie Zumeone/ref>

Disclaimer- Leitis-Goo`g Syndrome is better translated Googleitis Syndrome in English