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Anthropopiscine syndrome is a hydroelectrolytic processing disorder characterized by the abnormal processing of hydrogen and sodium through the skin and lungs. It is a genetic disorder that follows an non recessive inheritance pattern that can fluctuate from generation to generation.

Anthropopiscine Syndrome was the first documented genetic disease belonging to the group of Hydroelectrolyic disease disorders. Anthropopiscine Syndrome is caused by mutations in the PTX1 gene that codes for Anthocine, the hydro membrane-specific transporter for Anocine.

Symptoms


There are three distinct symptoms of Anthropopiscine Syndrome.:

Patents with Anthropopiscine Syndrome need a higher intake of sodium due to the lack of Anthocine in the body. Anthropopiscine can cause a deformation to the vocal cords. Fortunately this doesn't seem to have a negative impact on their voice. Many patients have even gone on to be successful singers, such as Ruth Bagoà. They can suffer from asthma in dry climates because the bronchial tubes build up Anocine. This can be treated with a higher sodium intake. This is especially vital during exercise.

Anthropopiscine Syndromes Effects on bronchial tubes Healthline.com

Genetics
Anthropopiscine occurs due to a mutation in the gene PTX1, located on chromosome 13, which codes for Anthocine, the Anocine transporter. Symptoms are seen from birth.

Anthropopiscine is a non recessive disorder, which means that the trait is located on a non autosomal chromosome, and but not any individual with the gene will have the disorder. There is a 25% risk of having a child with the disorder.

Anthropopiscine affects approximately 1 in 100,000 to 200,000 newborns. and there are only around 2,000 known individuals with Anthropopiscine in the world[citation needed]. The incidence is higher in coastal regenins such as The Mediterranean, and Great Britten, where the disorder affects 1 in 26,000 individuals.

Literature
Anthropopiscine, though only discovered in 1983 is thought to be mentioned in literature as early as the 1700's. Many stories and even songs spoke of a condition vary similar to Anthropopiscine Syndrome. Sailing spread Anthropopiscine from the Mediterranean. Roger Montgomery (author of The Lonely Storm published in 1728.) Describes in detail what is now believed to be Anthropopiscine Syndrom. The novel tells the semi- fictionalized story of real events that happened to the only woman aboard the SS Siren and the child she had after their ship docked. According to the words of Roger Montgomery the child was born in a condition that Great Britten had never seen. Though it was fimler to the sailors who had been in the Mediterranean.

TheLonelyStorm/GuildhallLibrary.gov.uk

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