Literature DB >> 8494858

Clinical features of affected males with X linked ocular albinism.

S J Charles1, J S Green, J W Grant, J R Yates, A T Moore.   

Abstract

Seventy four males affected by X linked ocular albinism (XLOA) from 19 pedigrees were examined to assess phenotypic variation and visual prognosis. Nystagmus was present in all cases except one. Best visual acuity ranged from 6/9 to 6/60; 79.7% could see 6/36 or better; most could read N5. Marked iris translucency and foveal hypoplasia were present in all cases. Posterior embryotoxon was present in 30% and dysplastic optic discs were often seen. Pigmentation of the posterior pole was associated with better visual acuity. XLOA is under-diagnosed: almost 20% of cases had been previously diagnosed as having congenital nystagmus until reviewed in this study.

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Year:  1993        PMID: 8494858      PMCID: PMC504486          DOI: 10.1136/bjo.77.4.222

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


  40 in total

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Journal:  Arch Ophthalmol       Date:  1976-01

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Journal:  Can J Ophthalmol       Date:  1971-10       Impact factor: 1.882

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Journal:  Can J Ophthalmol       Date:  1978-01       Impact factor: 1.882

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Journal:  Birth Defects Orig Artic Ser       Date:  1976

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Authors:  D Creel; F E O'Donnell; C J Witkop
Journal:  Science       Date:  1978-09-08       Impact factor: 47.728

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Journal:  Arch Ophthalmol       Date:  1978-07

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Authors:  A B Fulton; D M Albert; J L Craft
Journal:  Arch Ophthalmol       Date:  1978-02

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Journal:  Arch Ophthalmol       Date:  1976-11

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Authors:  F E O'Donnell; R A King; W R Green; C J Witkop
Journal:  Arch Ophthalmol       Date:  1978-09
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  23 in total

1.  Abnormal crossing of the optic fibres shown by evoked magnetic fields in patients with ocular albinism with a novel mutation in the OA1 gene.

Authors:  L Lauronen; R Jalkanen; J Huttunen; E Carlsson; S Tuupanen; S Lindh; H Forsius; E-M Sankila; T Alitalo
Journal:  Br J Ophthalmol       Date:  2005-07       Impact factor: 4.638

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Authors:  S M Carden; R E Boissy; P J Schoettker; W V Good
Journal:  Br J Ophthalmol       Date:  1998-02       Impact factor: 4.638

Review 3.  Recent advances in the gene map of inherited eye disorders: primary hereditary diseases of the retina, choroid, and vitreous.

Authors:  P J Rosenfeld; V A McKusick; J S Amberger; T P Dryja
Journal:  J Med Genet       Date:  1994-12       Impact factor: 6.318

4.  Carrier detection in X linked ocular albinism using linked DNA polymorphisms.

Authors:  S J Charles; A T Moore; Y Zhang; R McMahon; D E Barton; J R Yates
Journal:  Br J Ophthalmol       Date:  1994-07       Impact factor: 4.638

5.  Black diaphragm aniridia intraocular lens for aniridia and albinism.

Authors:  Victoria W Y Wong; Philip T H Lam; Timothy Y Y Lai; Dennis S C Lam
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2004-12-11       Impact factor: 3.117

6.  Deletion in the OA1 gene in a family with congenital X linked nystagmus.

Authors:  M Preising; J P Op de Laak; B Lorenz
Journal:  Br J Ophthalmol       Date:  2001-09       Impact factor: 4.638

7.  Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene loci.

Authors:  Y Zhang; R McMahon; S J Charles; J S Green; A T Moore; D E Barton; J R Yates
Journal:  J Med Genet       Date:  1993-11       Impact factor: 6.318

8.  X linked ocular albinism in Japanese patients.

Authors:  T Shiono; M Tsunoda; Y Chida; M Nakazawa; M Tamai
Journal:  Br J Ophthalmol       Date:  1995-02       Impact factor: 4.638

9.  Visual insignificance of the foveal pit: reassessment of foveal hypoplasia as fovea plana.

Authors:  Michael F Marmor; Stacey S Choi; Robert J Zawadzki; John S Werner
Journal:  Arch Ophthalmol       Date:  2008-07

10.  The ocular albinism type 1 gene product, OA1, spans intracellular membranes 7 times.

Authors:  Michio Sone; Seth J Orlow
Journal:  Exp Eye Res       Date:  2007-08-29       Impact factor: 3.467

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