Full-field electroretinograms in individuals with the Laurence-Moon-Bardet-Biedl syndrome

Acta Ophthalmologica Scandinavica

Volumn 74, Issue 6, 1996, Pages 618-620

  Riise, Ruth ^a   Andréasson, Sten ^b   Tornqvist, Kristina ^b  

^a Central Hospital of Hedmark   (Norway)

^b LUND UNIVERSITY HOSPITAL   (Sweden)

Author keywords

Full field electroretinograms; Laurence Moon Bardet Biedl syndrome; Tapetoretinal degeneration

Indexed keywords

ADOLESCENT; ADULT; AGING; ARTICLE; BARDET BIEDL SYNDROME; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; ELECTRORETINOGRAM; FEMALE; HUMAN; MALE; PRIORITY JOURNAL; RETINA CONE; RETINA DYSTROPHY; RETINA ROD; TAPETORETINAL DEGENERATION; VISUAL FIELD;

EID: 0030482582     PISSN: 13953907     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1600-0420.1996.tb00747.x     Document Type: Article

References (28)

1. Ammann F (1968): Investigations cliniques et génétiques sur le syndrome de Bardet-Biedl en Suisse. Thèse No 3045. Université de Genève.
2. Andréasson S. Ponjavic V & Ehinger B (1993): Full-field electro-retinogram in a patient with cutaneous melanoma - associated retinopathy. Acta Ophthalmol (Copenh) 71: 487-490.
3. Andréasson S, Sandberg M & Berson EL (1988): Narrow-band filtering for monitoring low-amplitude cone electro- retinograms in retinitis pigmentosa. Am J Ophthalmol 105: 500-503.
4. Bardet G (1920): Sur un syndrome d'obésité congénitale avec polydactylie et rétinite pigmentaire. (Contribution à l'étude des formes cliniques de l'obésité hypophysaire). These de Paris 470: 9-107.
5. Berson EL, Sandberg MA, Rosner B, Birch DG & Hansson AH (1985): Natural course of retinitis pigmentosa over a three-year interval. Am J Ophthalmol 99: 240-251.
6. Biedl A (1922): Ein Geschwisterpaar mit adiposo-genitaler Dystrophie. Dtsch Med Wochenschr 4: 1630.
7. Borgström MK, Ruse R, Tornqvist K & Granath L (1996): Anomalies in the permanent dentition and other oral findings in 29 individuals with Laurence-Moon-Bardet Biedl syndrome. J Oral Pathol Med 25: 86-89.
8. Campo RV & Aaberg TM (1982): Ocular and systemic manifestations of the Bardet-Biedl syndrome. Am J Ophthalmol 94: 750-756.
9. Churchill DN, McManamon P & Hurley RM (1981): Renal disease - a sixth cardinal feature of the Laurence-Moon-Biedl syndrome. Clin Nephrol 16: 151-154.
10. Fulton AB, Hansen RM & Glynn RJ (1993): Natural course of visual functions in the Bardet-Biedl Syndrome. Arch Ophthalmol 111: 1500-1506.
11. Green JS, Parfrey PS, Harnett JD, Farid NR, Cramer BC, Johnson G, Heath O, McManamon PJ, O'Leary E & Pryse- Phillips W (1989): The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome. N Engl J Med 321: 1002-1009.
12. Harnett JD, Green JS, Cramer BC, Johnson G, Chafe L, McManamon P, Farid NR, Pryse-Phillips W & Parfrey PS (1988): The spectrum of renal disease in Laurence-Moon-Biedl syndrome. N Engl J Med 319: 615-618.
13. Harrison JM & v Heuven WAJ (1985): Rodcone interactions in the ERG of a patient with Bardet-Biedl syndrome. Doc Ophthalmol 60: 203-209.
14. Hutchinson J (1900): Slowly progressive paraplegia and disease of the chorioids with defective intellect and arrested sexual development in several brothers and a sister. Arch Surg 11: 118-122.
15. Iannaccone A, Vingolo EM, Rispoli E, De Propris G, Tanzilli P & Pannarale MR (1996): Electroretinographic alterations in the Laurence-Moon-Bardet-Biedl phenotype. Acta Ophthalmol Scand 74: 8-13.
16. Jacobson SG, Borruat F-X & Apathy PP (1990): Patterns of rod and cone dysfunction in Bardet-Biedl Syndrome. Am J Ophthalmol 109: 676-688.
17. Kobrin JL, Ternand CL, Knobloch WH & Johnsson DD (1990): Dental abnormalities as a component of the Laurence-Moon-Bardet-Biedl syndrome. Ophthalm Paediatr Genet 11: 299-303.
18. Krill AE, Folk E & Rosenthal IM (1961): Electroretinography in the Laurence-Moon-Biedl Syndrome. Am J Dis Child 102: 205-209.
19. Laurence JC & Moon RC (1866): Four cases of 'Retinitis Pigmentosa' occurring in the same family, and accompanied by general imperfections of development. Ophthalmol Rev 2: 32-41.
20. Lavy T, Harris CM, Shawkat F, Thompson D & Taylor D (1995): Electrophysiological and eye-movement abnormalities in children with the Bardet-Biedl syndrome. J Pedi atr Ophthalmol Strabismus 32: 364-367.
21. Leys MJ, Schreiner LA, Hansen RM, Mayer L & Fulton AB (1988): Visual acuities and dark-adapted thresholds of children with Bardet-Biedl Syndrome. Am J Ophthalmol 106: 561-569.
22. Lofterød B, Ruse R, Skuseth T & Storhaug K (1990): Laurence- Moon-Bardet-Biedl syndrom. Nord Med 105: 146-148.
23. Ruse R (1987): Visual function in Laurence-Moon-Bardet-Biedl syndrome. A survey of 26 cases. Acta Ophthalmol (Copenh) Suppl 182: 128-131.
24. Riise R, Tornqvist K, Andréasson S, Borgström M, Rydling O & Ehinger B (1995) : Inter- and intrafamilial variation of the phenotype in Laurence-Moon-Bardet-Biedl (LMBB) syndrome. Invest Ophthalmol Vis Sci 36(4): 874.
25. Riise R, Andréasson S, Wright AF & Tornqvist K (1996): Ocular findings in the Laurence-Moon-Bardet-Biedl syndrome. Acta Ophthalmol Scand 74: 612-617.
26. Rizzo JF, Berson EL & Lessell S (1986): Retinal and neurologic findings in the Laurence-Moon-Bardet-Biedl syndrome. Ophthalmology 93: 1452-1456.
27. Schachat AP & Maumenee I H (1982): Bardet-Biedl syndrome and related disorders. Arch Ophthalmol 100: 285-288.
28. Stanescu B & Wawernia E (1970):Electroretinograms and electroencephalograms in Laurence-Moon-Bardet-Biedl syndrome. Confin Neurol 32: 423-435.