Literature DB >> 3261411

Diagnosis of dominant infantile optic atrophy in early childhood.

W Jaeger1.   

Abstract

An acquired tritan defect is the earliest and the most pathognomonic sign of dominant infantile optic atrophy (DIOA) and the Tritan Album of Lanthony (1985) is helpful for the diagnosis of this condition. In preschool children, diagnosis of DIOA is possible by modifications of this test, using one plate under standard illumination which can be rotated into four positions, and by measuring the maximum distance of recognition of the plate.

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Year:  1988        PMID: 3261411     DOI: 10.3109/13816818809031474

Source DB:  PubMed          Journal:  Ophthalmic Paediatr Genet        ISSN: 0167-6784


  2 in total

Review 1.  Clinical features, molecular genetics, and pathophysiology of dominant optic atrophy.

Authors:  M Votruba; A T Moore; S S Bhattacharya
Journal:  J Med Genet       Date:  1998-10       Impact factor: 6.318

2.  Clinical heterogeneity of dominant optic atrophy: the contribution of visual function investigations to diagnosis.

Authors:  G Del Porto; E M Vingolo; K Steindl; R Forte; A Iannaccone; E Rispoli; M R Pannarale
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1994-12       Impact factor: 3.117

  2 in total

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