BMJ · 1986 · 33 citations · 6 references
Life SciencesBiochemistryGeneticsEnzymologyMetabolismNeuro-ophthalmologyEnzyme DeficienciesHereditary NeuropathiesInborn Errors Of MetabolismOptic NeuropathiesCyanide MetabolismDetoxication MechanismsGastrointestinal MucosaInherited Optic NeuropathiesLeber Hereditary Optic Neuropathy
Leber's hereditary optic neuropathy is a rare cause of progressive visual failure. Its cause is unknown, but one hypothesis is that patients have a defect in the detoxication of cyanide. One of the enzymes used in this detoxication is thiosulphate sulphurtransferase (rhodanese). The activity of this enzyme was measured in the rectal mucosa of a group of subjects with Leber's hereditary optic neuropathy, and it was found to be considerably reduced compared with that in a group of controls (p less than 0.001). This finding supports the hypothesis of an inborn error of cyanide detoxication in this condition.
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Crystalline Rhodanese. I. Purification and Physicochemical Examination.
Bo Sörbo, Ulf Lagerkvist, Rainer Pesola et al. · Acta chemica Scandinavica/Acta chemica Scandinavica. B, Organic chemistry and biochemistry/Acta chemica Scandinavica. A, Physical and inorganic chemistry/Acta chemica Scandinavica. Series B. Organic chemistry and biochemistry/Acta chemica Scandinavica. Series A, Physical and inorganic chemistry · 1953 · 313 citations · Full text
Ophthalmoscopic Findings in Leber's Hereditary Optic Neuropathy
Eeva Nikoskelainen · Archives of Ophthalmology · 1983 · 147 citations
Medicine, Neurology, Ophthalmology +16
Leber's hereditary optic atrophy: a possible defect of cyanide metabolism.
John Wilson · PubMed · 1965 · 99 citations
Medicine, Genetics, Ophthalmology +11
PLASMA-COBALAMINS IN NEURO-OPHTHALMOLOGICAL DISEASES
John Wilson, J. C. Linnell, D. M. Matthews · The Lancet · 1971 · 48 citations
Medicine, Neurology, Ophthalmology +11