• Thumbnail for Aminolevulinic acid dehydratase deficiency porphyria
    Aminolevulinic acid dehydratase deficiency porphyria (also known as Doss porphyria, plumboporphyria, or ADP) is an extremely rare autosomal recessive metabolic...
    10 KB (972 words) - 21:09, 18 July 2024
  • Thumbnail for Porphyria
    (AIP), variegate porphyria (VP), aminolevulinic acid dehydratase deficiency porphyria (ALAD), hereditary coproporphyria (HCP), and porphyria cutanea tarda...
    64 KB (6,616 words) - 16:14, 3 August 2024
  • Thumbnail for Delta-aminolevulinic acid dehydratase
    Aminolevulinic acid dehydratase (porphobilinogen synthase, or ALA dehydratase, or aminolevulinate dehydratase) is an enzyme (EC 4.2.1.24) that in humans...
    17 KB (1,918 words) - 18:27, 25 July 2024
  • Thumbnail for Porphyrin
    formation of δ-aminolevulinic acid (δ-ALA, 5-ALA or dALA) by the reaction of the amino acid glycine with succinyl-CoA from the citric acid cycle. In plants...
    25 KB (2,304 words) - 16:20, 3 August 2024
  • E, et al. (September 2018). "5,10-methenyltetrahydrofolate synthetase deficiency causes a neurometabolic disorder associated with microcephaly, epilepsy...
    43 KB (983 words) - 04:37, 11 August 2024
  • Thumbnail for List of skin conditions
    disease) Alkaptonuria Aminolevulinic acid dehydratase deficiency porphyria (Doss porphyria, plumboporphyria) B-mannosidase deficiency Carotenosis Cerebral...
    198 KB (17,958 words) - 01:24, 6 July 2024
  • Thumbnail for Heme
    pathway for making heme: ALAD: aminolevulinic acid, δ-, dehydratase (deficiency causes ala-dehydratase deficiency porphyria) ALAS1: aminolevulinate, δ-,...
    42 KB (4,371 words) - 08:01, 7 June 2024
  • Society Dioctyl sodium sulfosuccinate Doss porphyria, aminolevulinic acid dehydratase deficiency porphyria Search for "doss" on Wikipedia. Dos (disambiguation)...
    2 KB (231 words) - 07:22, 29 April 2024
  • Thumbnail for Lead poisoning
    interferes with the activity of an essential enzyme called delta-aminolevulinic acid dehydratase, or ALAD (see image of the enzyme structure), which is important...
    198 KB (21,307 words) - 23:33, 13 July 2024
  • Thumbnail for Tyrosinemia type I
    Tyrosinemia type I (category Amino acid metabolism disorders)
    to secondary effects. SA inhibits the enzyme 5-ALA dehydratase which converts aminolevulinic acid (5-ALA) into porphobilinogen, a precursor to porphyrin...
    30 KB (3,369 words) - 09:15, 17 November 2023