hawkinsin

hawkinsin
haw·kin·sin (hawґkin-sin) a cyclic amino acid metabolite of tyrosine excreted in hawkinsinuria, a rare aminoacidopathy. It is formed from an intermediate of the 4-hydroxyphenylpyruvate dioxygenase reaction combined with glutathione.

Medical dictionary. 2011.

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  • Hawkinsin — chembox new ImageFile=Hawkinsin.png ImageSize=200px IUPACName= 2 Amino 3 [2 (carboxymethyl) 2,5 dihydroxy 1 cyclohex 3 enyl] sulfanyl] propanoic acid OtherNames=(2 L Cystein S yl 1,4 dihydroxycyclohex 5 en 1 yl)acetic acid Section1=Chembox… …   Wikipedia

  • Hawkinsinuria — Infobox Disease Name = PAGENAME Caption = Hawkinsin DiseasesDB = 29836 ICD10 = ICD9 = ICDO = OMIM = 276710 OMIM mult = OMIM2|140350 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = D020176 Hawkinsinuria, also called 4 Alpha… …   Wikipedia

  • ТИРОЗИНЕМИЯ — мед. Тирозинемия повышенная концентрация тирозина в крови приводит к увеличению выделения с мочой соединений тирозина, гепатоспленомегалии, узловому циррозу печени, множественным дефектам почечной канальцевой реабсорбции и витамин D резистентному …   Справочник по болезням

  • hawkinsinuria — haw·kin·sin·u·ria (haw″kin sin uґre ə) a rare autosomal dominant disorder caused by heterozygous mutation in the HPD gene (locus: 12q24 qter), which encodes 4 hydroxyphenylpyruvate dioxygenase, an enzyme important in tyrosine… …   Medical dictionary

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