IN a recent publication1, Kurogi reports the existence of a Conchocelis-phase in the life-history of four Japanese species of Porphyra. He confirms my observations on the germination of the spores
Porphyria cutanea tarda can be genetically inherited in families. However, in most people affected there is no family history. In these susceptible people it can be triggered by exposure to certain medicines or chemicals, including oral contraceptives and alcohol. Porphyria cutanea tarda can also sometimes occur if you have another illness Porphyria is an inherited rare disorder that affects the nervous system or skin and may cause abdominal pain. Cells of porphyria patients are unable to change body chemicals called porphyrins and its precursors into heme, the substance responsible for blood color. Skin symptoms characterize the biochemically and clinically manifest stage. Latent or subclinical phases in which urinary porphyrin constellations change from mild to severe stages can be recognized before cutaneous lesions arise. The development of chronic hepatic porphyria is outlined in Figure 2. 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The cultivation of nori is a substantial industry; Dulse is eaten in regions surrounding the North Atlantic. Cheryl Greenacre, in Small Animal Dermatology (Fourth Edition), 2017 “Sore Nose” or Porphyrin Irritation—Gerbil Features. Porphyrin tears occur in gerbils because of stress from excess Harderian gland secretions, which contain red porphyrins that look like blood. In gerbils, this material is particularly irritating and is associated with nose rubbing on the cage and secondary trauma. Acute intermittent porphyria (AIP) is characterized by attacks of abdominal pain and neuropsychiatric symptoms. In northern Sweden, about half of those patients carrying the gene encoding for this condition have experienced attacks with abdominal pain, more frequently and more severely affecting women. In biochemical terms, AIP is an autosomal hereditary metabolic aberration resulting from a Porphyria cutanea tarda can be genetically inherited in families. However, in most people affected there is no family history. In these susceptible people it can be triggered by exposure to certain medicines or chemicals, including oral contraceptives and alcohol. Porphyria cutanea tarda can also sometimes occur if you have another illness Porphyria is an inherited rare disorder that affects the nervous system or skin and may cause abdominal pain. Cells of porphyria patients are unable to change body chemicals called porphyrins and its precursors into heme, the substance responsible for blood color. Skin symptoms characterize the biochemically and clinically manifest stage. Latent or subclinical phases in which urinary porphyrin constellations change from mild to severe stages can be recognized before cutaneous lesions arise. The development of chronic hepatic porphyria is outlined in Figure 2. 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