Monday , September 26 2022

A rare childhood disorder worries the United States



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The US authorities said they ignored the direct cause of a rare chance of childhood illness in the country, acute, flaky paralysis, close to polio.

Acute flaccid paralysis (AFP) is a rare but serious patient. Characterized by acute inflammation of the spinal cord cells, it is close to polio (polio) as it can cause paralysis that affects the arms or legs. In the United States, the number of cases increases sharply. A situation that worries parents very much. On November 13, US authorities also acknowledged ignoring the direct cause of this pathology.

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Children aged between 2 and 8 years are the most affected. Three to ten days before they suffered from paralysis, they all complained of fever and respiratory problems. Centers for Disease Control and Prevention (CDC) studied 125 cases, and half of them were positive for an enterovirus or rhinovirus, causing fever, clogged nose, vomiting, diarrhea and pain. muscle. But scientists still do not know the exact cause of the disease. CDC is an agency that works with science and science does not respond at present ", Nancy Messonier, director of the organization, told AFP retransmitted Le Figaro.

A total of 252 children were treated for AFP symptoms this year. Since last week, even 33 new cases have been reported. With 80 confirmed patients, "It seems that we are heading towards a year in phase with the last two years of peak (149 cases in 2016 and 120 cases in 2014)", she said. The syndrome began in 2014, but only about ten cases were recorded in 2015 and 2017.

Some of the children with AFP have recovered quickly and many have remained paralyzed. Because the disease directly affects the nervous system. In 2017, a child died in the United States. There is today a specific treatment for this pathology. Nancy Messonier assured, however, that the disease remained rare. The researcher invites parents "Call immediate medical attention for children who have a sudden weakness in their arms and legs".

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