Matches in DBpedia 2016-04 for { ?s ?p "Aminolevulinic acid dehydratase deficiency porphyria (also known as \"Doss porphyria,\" and \"Plumboporphyria\") is a cutaneous condition, disease can present during early childhood (as well as in adulthood) with acute neurologic symptoms that resemble those encountered in acute intermittent porphyria. The condition is extremely rare, with fewer than 10 cases ever reported.ALA dehydratase deficiency is a rare cause of hepatic porphyria. It is an autosomal recessive disorder that results from inappropriately low levels of the enzyme ALA dehydratase (ALAD, also called porphobilinogen synthase), which is required for normal heme synthesis."@en }
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- Aminolevulinic_acid_dehydratase_deficiency_porphyria abstract "Aminolevulinic acid dehydratase deficiency porphyria (also known as \"Doss porphyria,\" and \"Plumboporphyria\") is a cutaneous condition, disease can present during early childhood (as well as in adulthood) with acute neurologic symptoms that resemble those encountered in acute intermittent porphyria. The condition is extremely rare, with fewer than 10 cases ever reported.ALA dehydratase deficiency is a rare cause of hepatic porphyria. It is an autosomal recessive disorder that results from inappropriately low levels of the enzyme ALA dehydratase (ALAD, also called porphobilinogen synthase), which is required for normal heme synthesis.".