• 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...
    11 KB (1,149 words) - 23:17, 20 August 2023
  • 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) - 17:46, 24 June 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) - 08:30, 2 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 (2,307 words) - 17:29, 21 February 2024
  • E, et al. (September 2018). "5,10-methenyltetrahydrofolate synthetase deficiency causes a neurometabolic disorder associated with microcephaly, epilepsy...
    42 KB (969 words) - 16:02, 3 April 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 (21,295 words) - 04:02, 10 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