Dominant optic atrophy mapped to chromosome 3q region: II. Clinical and epidemiological aspects

Acta Ophthalmologica Scandinavica

Volumn 74, Issue 1, 1996, Pages 3-7

  Kjer, Birgit ^a   Eiberg, Hans ^b   Kjer, Poul ^c   Rosenberg, Thomas ^c  

^a HVIDOVRE HOSPITAL   (Denmark)

^b UNIVERSITY OF COPENHAGEN   (Denmark)

^c National Eye Clinic for the Visually Impaired Denmark   (Denmark)

Author keywords

Chromosome 3; Dominant optic atrophy; Hereditary optic atrophy; Linkage analysis; Prevalence rate

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHILD; CHROMOSOME 3Q; FEMALE; FOLLOW UP; GENE MAPPING; GENETIC LINKAGE; HEREDITARY OPTIC ATROPHY; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; VISUAL ACUITY; VISUAL IMPAIRMENT;

ADOLESCENT; ADULT; AGED; CHILD; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 3; DENMARK; FEMALE; FOLLOW-UP STUDIES; GENETIC MARKERS; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; MIDDLE AGED; OPTIC ATROPHIES, HEREDITARY; PEDIGREE; PREVALENCE; RETROSPECTIVE STUDIES; RISK FACTORS; VISUAL ACUITY;

EID: 0029924084     PISSN: 13953907     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1600-0420.1996.tb00672.x     Document Type: Article

References (25)

1. Eiberg H, Kjer B, Kjer P & Rosenberg T (1994): Dominant optic atrophy mapped to chromosome 3q region. I Linkage analysis. Hum Mol Genet 3: 977-980.
2. Eliott D, Traboulsi EI & Maumenee IH (1993): Visual prognosis in autosomal dominant optic atrophy. Am J Ophthal 115: 360-367.
3. Grützner P (1966): Koppelungsuntersuchungen bei der infantilen,dominant vererbten Opticus-Atrophie. Human-genetik 2: 363-371.
4. Gyapay G, Morissette J, Vignal A, Dip C, Fizames C, Millasseau P, Marc S, Benardi G, Lathrop M & Weissenbach J (1994): The 1993-1994 Genethon human genetic linkage map. Nature Genet 7: 246-339.
5. Harding GFA & Crews SJ (1982): The visual evoked potential in hereditary optic atrophy. Clinical application of evoked potentials in neurology. 21-30. Raven Press, New York.
6. Hoyt CS (1980): Autosomal dominant optic atrophy. Ophthalmology 87: 245-250.
7. Jaeger W (1954): Dominant vererbte Opticusatrophie. Graefes Arch Ophthalmol 155: 457-484.
8. Jaeger W (1966): Hereditary optic atrophies in childhood. J Genet Hum 15: 312-319.
9. Jaeger W (1988): Diagnosis of dominant infantile optic atrophy in early childhood. Ophthal Ped Genet 9: 7-11.
10. Johnston PB, Gaster RN, Smith VC & Ramesh CT (1979): A clinicopathologic study of autosomal dominant optic atrophy. Am J Ophthalmol 88: 868-875.
11. Kivlin JD, Lovrien EW, Bishop T & Maumenee IH (1983): Linkage analysis in dominant optic atrophy. Am J Hum Genet 35: 1190-1195.
12. Kjer P (1956): Hereditary infantile optic atrophy with dominant transmission. Danish Med Bull 3: 135-141.
13. Kjer P (1959): Infantile optic atrophy with dominant mode of inheritance. Acta Ophthalmol (Copenh) 37: Suppl 54: 1-146.
14. Kjer R Jensen OA & Klinken L (1983): Histopathology of eye, optic nerve and brain in a case of dominant optic atrophy. Acta Ophthalmol (Copenh) 61:300-312.
15. Kline LB & Glaser JS (1979): Dominant optic atrophy. Arch Ophthalmol 97: 1680-1686.
16. Krill AE, Smith VC & Pokorny J (1970): Similarities between congenital tritan defects and dominant optic nerve atrophy. J Opt Soc Am 60: 1132-1139.
17. Lathrop GM & Lalouel JM (1984): Easy calculations of lod scores and genetic risks on small computers. Am J Hum Genet 36: 460-465.
18. Lodberg CV & Lund A (1950): Hereditary optic atrophy with dominant transmission. Acta Ophthalmol (Copenh) 28: 437-468.
19. Lyle WM (1990): Genetic Risks. 4-36. University of Waterloo Press, Waterloo, Ontario.
20. Meire F, de Laey JJ, de Bie S, van Staey M & Matton MT (1985): Dominant optic nerve atrophy with progressive hearing loss and chronic progressive external ophthalmoplegia. Opthal Ped and Genet 5: 91-97.
21. Mets MB & Mhoon E (1985): Probable autosomal dominant optic atrophy with hearing loss. Opthal Ped and Genet 5:85-89.
22. Papst N, Bopp M & Wundrack EM (1985): Muster-ERG und muster-VECP bei autosomal dominanter infantiler Optikusatrophie. Fortschr Ophthalmol 82: 300-301.
23. Shapiro LR, Raab EL, Leopold IH & Hirschhorn K (1969): Hereditary optic atrophy. Arch Ophthal 81: 359-362.
24. Smith DP (1972): Diagnostic criteria in dominantly inherited juvenile optic atrophy. Am J of Optom and Arch of Am Acad of Optom 49: 183-200.
25. Weissenbach J, Gyapay G, Dib C, Vignal A, Morissette J, Millasseau P, Vaysseix G & Lathrop M (1992): A second generation linkage map of the human genome. Nature 359: 794-801.