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Porphyria has been suggested as an explanation for the origin of vampire and werewolf legends, based upon certain perceived similarities between the condition and the folklore. In January 1964, L. Illis's 1963 paper 'On Porphyria and the Aetiology of Werewolves' was published in Proceedings of the Royal Society of Medicine.
Porphyria, a group of diseases in which substances called porphyrins build up; Vampirism, a term describing being a vampire This page was last edited on 30 ...
Porphyria cutanea tarda is the most common subtype of porphyria. [1] The disease is named because it is a porphyria that often presents with skin manifestations later in life. The disorder results from low levels of the enzyme responsible for the fifth step in heme production. Heme is a vital molecule for all of the body's organs.
Erythropoietic protoporphyria (or commonly called EPP) is a form of porphyria, which varies in severity and can be very painful.It arises from a deficiency in the enzyme ferrochelatase, leading to abnormally high levels of protoporphyrin in the red blood cells (erythrocytes), plasma, skin, and liver. [2]
The Vampire, by Philip Burne-Jones, 1897. A vampire is a mythical creature that subsists by feeding on the vital essence (generally in the form of blood) of the living.In European folklore, vampires are undead humanoid creatures that often visited loved ones and caused mischief or deaths in the neighbourhoods which they inhabited while they were alive.
Acute intermittent porphyria (AIP) is a rare metabolic disorder affecting the production of heme resulting from a deficiency of the enzyme porphobilinogen deaminase. It is the most common of the acute porphyrias .
Considering that the Vampire legends and the Blood letting had no link with the Porphyric part of the Vampire stories. They are two separate things. The Porphyric part of the Vampire legends should be completely obvious to anyone, the sunlight part of the stories are really the only part dealing with Porphyria.
Variegate porphyria is inherited in an autosomal dominant pattern, which means the defective gene is located on an autosome, and inheriting one copy of the defective gene from an affected parent is sufficient to cause the disorder. More severe cases result from inheriting two copies of the defective gene.