Literature DB >> 2729274

Color vision defects in adrenomyeloneuropathy.

G H Sack1, M B Raven, H W Moser.   

Abstract

The relationship between abnormal color vision and adrenomyeloneuropathy (AMN) was investigated in 27 AMN patients and 31 age-matched controls by using the Farnsworth-Munsell 100 Hue test. Twelve (44%) of 27 patients showed test scores significantly above normal. The axes of bipolarity determined by the testing differed widely between the patients with abnormal scores, compatible with the notion that different alterations in visual pigment genes occur in different AMN kindreds. These observations confirm our earlier impression that the frequency of abnormal color vision is increased in these kindreds, and it supports our contentions that (1) AMN (and its companion, adrenoleukodystrophy) are very closely linked to the visual pigment loci at Xq28 and (2) this proximity might provide the opportunity to observe contiguous gene defects.

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Year:  1989        PMID: 2729274      PMCID: PMC1715662     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  23 in total

1.  Further studies on acquired deficiency of color discrimination.

Authors:  G VERRIEST
Journal:  J Opt Soc Am       Date:  1963-01

Review 2.  Contiguous gene syndromes: a component of recognizable syndromes.

Authors:  R D Schmickel
Journal:  J Pediatr       Date:  1986-08       Impact factor: 4.406

3.  Molecular genetics of inherited variation in human color vision.

Authors:  J Nathans; T P Piantanida; R L Eddy; T B Shows; D S Hogness
Journal:  Science       Date:  1986-04-11       Impact factor: 47.728

4.  Proposals for scoring and assessing the 100-Hue test.

Authors:  P R Kinnear
Journal:  Vision Res       Date:  1970-05       Impact factor: 1.886

5.  Assignment of the gene for dyskeratosis congenita to Xq28.

Authors:  J M Connor; D Gatherer; F C Gray; L A Pirrit; N A Affara
Journal:  Hum Genet       Date:  1986-04       Impact factor: 4.132

6.  Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy.

Authors:  L M Kunkel; J F Hejtmancik; C T Caskey; A Speer; A P Monaco; W Middlesworth; C A Colletti; C Bertelson; U Müller; M Bresnan; F Shapiro; U Tantravahi; J Speer; S A Latt; R Bartlett; M A Pericak-Vance; A D Roses; M W Thompson; P N Ray; R G Worton; K H Fischbeck; P Gallano; M Coulon; C Duros; J Boue; C Junien; J Chelly; G Hamard; M Jeanpierre; M Lambert; J C Kaplan; A Emery; H Dorkins; S McGlade; K E Davies; C Boehm; B Arveiler; C Lemaire; G J Morgan; M J Denton; J Amos; M Bobrow; F Benham; E Boswinkel; C Cole; V Dubowitz; K Hart; S Hodgson; L Johnson; A Walker; L Roncuzzi; A Ferlini; C Nobile; G Romeo; D E Wilcox; N A Affara; M A Ferguson-Smith; M Lindolf; H Kaariainen; A de la Chapelle; V Ionasescu; C Searby; R Ionasescu; E Bakker; G J van Ommen; P L Pearson; C R Greenberg; J L Hamerton; K Wrogemann; R A Doherty; R Polakowska; C Hyser; S Quirk; N Thomas; J F Harper; B T Darras; U Francke
Journal:  Nature       Date:  1986 Jul 3-9       Impact factor: 49.962

7.  Lignoceroyl-CoASH ligase: enzyme defect in fatty acid beta-oxidation system in X-linked childhood adrenoleukodystrophy.

Authors:  M Hashmi; W Stanley; I Singh
Journal:  FEBS Lett       Date:  1986-02-17       Impact factor: 4.124

8.  Identification of female carriers of adrenoleukodystrophy.

Authors:  H W Moser; A E Moser; J E Trojak; S W Supplee
Journal:  J Pediatr       Date:  1983-07       Impact factor: 4.406

9.  Electroretinograms in carriers of blue cone monochromatism.

Authors:  E L Berson; M A Sandberg; A Maguire; W C Bromley; T H Roderick
Journal:  Am J Ophthalmol       Date:  1986-08-15       Impact factor: 5.258

10.  Adrenoleukodystrophy: survey of 303 cases: biochemistry, diagnosis, and therapy.

Authors:  H W Moser; A E Moser; I Singh; B P O'Neill
Journal:  Ann Neurol       Date:  1984-12       Impact factor: 10.422

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  9 in total

Review 1.  Ophthalmic manifestations of inherited neurodegenerative disorders.

Authors:  Hannah M Kersten; Richard H Roxburgh; Helen V Danesh-Meyer
Journal:  Nat Rev Neurol       Date:  2014-05-20       Impact factor: 42.937

2.  X-linked adrenoleukodystrophy and haemophilia A in the same kindred.

Authors:  A Nogueira; P Jorge; J Dores; M Cunha; S Sousa; I Pereira; M Campos; B Justiça; D Quelhas; M Sá Miranda
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

3.  Chromosomal rearrangement segregating with adrenoleukodystrophy: a molecular analysis.

Authors:  G H Sack; M Alpern; T Webster; R P Feil; J C Morrell; G Chen; W Chen; C T Caskey; H W Moser
Journal:  Proc Natl Acad Sci U S A       Date:  1993-10-15       Impact factor: 11.205

Review 4.  DNA diagnosis of X-linked adrenoleukodystrophy.

Authors:  S Seneca; W Lissens
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

Review 5.  Adrenoleukodystrophy: phenotypic variability and implications for therapy.

Authors:  H W Moser; A B Moser; K D Smith; A Bergin; J Borel; J Shankroff; O C Stine; C Merette; J Ott; W Krivit
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

6.  Chromosomal rearrangement segregating with adrenoleukodystrophy: associated changes in color vision.

Authors:  M Alpern; G H Sack; D H Krantz; J Jenness; H Zhang; H W Moser
Journal:  Proc Natl Acad Sci U S A       Date:  1993-10-15       Impact factor: 11.205

7.  The red-green visual pigment gene region in adrenoleukodystrophy.

Authors:  P Aubourg; R Feil; S Guidoux; J C Kaplan; H Moser; A Kahn; J L Mandel
Journal:  Am J Hum Genet       Date:  1990-03       Impact factor: 11.025

8.  Adrenoleukodystrophy: a complex chromosomal rearrangement in the Xq28 red/green-color-pigment gene region indicates two possible gene localizations.

Authors:  R Feil; P Aubourg; J Mosser; A M Douar; D Le Paslier; C Philippe; J L Mandel
Journal:  Am J Hum Genet       Date:  1991-12       Impact factor: 11.025

Review 9.  Dysfunctional peroxisomal lipid metabolisms and their ocular manifestations.

Authors:  Chuck T Chen; Zhuo Shao; Zhongjie Fu
Journal:  Front Cell Dev Biol       Date:  2022-09-07
  9 in total

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