Acute exudative polymorphous vitelliform maculopathy syndrome

Retina

Volumn 23, Issue 4, 2003, Pages 453-462

  Chan, Clement K ^a,b   Gass, J Donald M ^c   Lin, Steven G ^a  

^a S California Desert Retina Consult   (United States)

^b LOMA LINDA UNIVERSITY   (United States)

^c VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PERIPHERIN; PREDNISONE;

ACUTE DISEASE; ACUTE EXUDATIVE POLYMORPHOUS VITELLIFORM MACULOPATHY SYNDROME; ADULT; ARTICLE; CASE REPORT; CLINICAL FEATURE; COLOR VISION; COXSACKIE VIRUS; DARK ADAPTATION; ELECTROOCULOGRAPHY; ELECTRORETINOGRAPHY; EVOKED VISUAL RESPONSE; FEMALE; FLUORESCENCE ANGIOGRAPHY; HEADACHE; HUMAN; OPTICAL COHERENCE TOMOGRAPHY; PIGMENT EPITHELIUM; RETINA DETACHMENT; RETINA MACULOPATHY; SYMPTOM; SYNDROME; UPPER RESPIRATORY TRACT INFECTION; VISUAL ACUITY; VISUAL IMPAIRMENT;

ACUTE DISEASE; ELECTROPHYSIOLOGY; EXUDATES AND TRANSUDATES; FEMALE; FLUORESCEIN ANGIOGRAPHY; HUMANS; MIDDLE AGED; OPHTHALMOSCOPY; PIGMENT EPITHELIUM OF EYE; RETINA; RETINAL DETACHMENT; RETINAL DISEASES; SYNDROME; TOMOGRAPHY, OPTICAL COHERENCE;

EID: 0041836112     PISSN: 0275004X     EISSN: None     Source Type: Journal    
DOI: 10.1097/00006982-200308000-00002     Document Type: Article

References (25)

1. Gass JDM, Chuang EL, Granek H. Acute exudative polymorphous vitelliform maculopathy. Trans Am Ophthalmol Soc 1988;86:354-366.
2. Gass JDM. Acute idiopathic exudative polymorphous vitelliform maculopathy. In: Gass JDM, ed. Stereoscopic atlas of macular diseases: diagnosis and treatment, 4th ed. St Louis: CV Mosby, 1997:168-169, vol 1, 696-697, vol 2.
3. Lotery AJ, Munier FL, Fishman GA, et al. Allelic variation in the VMD2 gene in Best disease and age-related macular degeneration. Invest Ophthalmol Vis Sci 2000;41:1291-1296.
4. Kraushar MF, Margolis S, Morse PH, Nugent ME. Pseudohypopyon in Best's vitelliform macular dystrophy. Am J Ophthalmol 1982;94:30-33.
5. Lopez PF, Maumenee IH, de la Cruz Z, Green WR. Autosomal-dominant fundus flavimaculatus: clinicopathologic correlation. Ophthalmology 1990;97:798-809.
6. Miller SA. Fluorescence in Best's vitelliform dystrophy, lipofuscin, and fundus flavimaculatus. Br J Ophthalmol 1978;62:256-260.
7. Gass JDM. Exudation and fluorescein staining, mechanisms of serous and hemorrhagic disciform detachment of the macula, specific diseases causing disciform macular detachment, age-related macular degeneration. In: Gass JDM, ed. Stereoscopic atlas of macular diseases: diagnosis and treatment, 4th ed, vol 1. St Louis: CV Mosby, 1997:24-45, 49-71, 72-105.
8. Ryan SJ, Maumenee AE. Birdshot retinochoroidopathy. Am J Ophthalmol 1980;89:31-45.
9. Gass JDM. Vitiliginous chorioretinitis. Arch Ophthalmol 1981;99:1778-1787.
10. Nussenblatt RB, Mittal KK, Ryan S, et al. Birdshot retinochoroidopathy associated with HLA-A29 antigen and immune responsiveness to retinal S-antigen. Am J Ophthalmol 1982;94:147-158.
11. Miller SA. Multifocal Best's vitelliform dystrophy. Arch Ophthalmol 1977;95:984-5990.
12. Cross HE, Bard L. Electro-oculography in Best's macular dystrophy. Am J Ophthalmol 1974;77:46-50.
13. Musarella MA. Molecular genetics of macular degeneration. Documenta Ophthalmol 2001;102:165-177.
14. Petrukhin K, Koisti MJ, Bakall B, et al. Identification of the gene responsible for Best macular dystrophy. Nat Genet 1998;19:241-247.
15. Bakall B, Marknell T, Ingvast S, et al. The mutation spectrum of the bestrophin protein-functional implications. Hum Genet 1999;104:383-389.
16. Nichols BE, Drack AV, Vandenburgh K, et al. A2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea. Hum Mol Genet 1993;2:1347.
17. Hoyng CB, Heutink P, Testers L, et al. Autosomal dominant central areolar choroidal dystrophy caused by a mutation in codon 142 in the peripherin/RDS gene. Am J Ophthalmol 1996;121:623-629.
18. Dryja TP, Hahn LB, Kajiwara K, Berson EL. Dominant and digenic mutations in the peripherin/RDS and ROM1 genes in retinitis pigmentosa. Invest Ophthalmol Vis Sci 1997;38:1972-1981.
19. Kemp CM, Jacobson SG, Cideciyan AV, et al. RDS gene mutations causing retinitis pigmentosa or macular degeneration lead to the same abnormality in photoreceptor function. Invest Ophthalmol Vis Sci 1994;35:3154-3162.
20. Gass JDM. Harada's disease. In: Gass JDM, ed. Stereoscopic atlas of macular diseases: diagnosis and treatment, 4th ed, vol 1. St Louis: CV Mosby, 1997:176-180.
21. Gass JDM, Sever RJ, Grizzard WS, et al. Multifocal pigment epithelial detachments by reticulum cell sarcoma; a characteristic funduscopic picture. Retina 1984;4:135-143.
22. Gass JDM. Retinal and uveal tract involvement with the lymphomas. In: Gass JDM, ed, Stereoscopic atlas of macular diseases: diagnosis and treatment, 4th ed, volume 2. St Louis: CV Mosby, 1997:880-888.
23. Gass JDM. Bilateral diffuse uveal melanocytic proliferation associated with systemic carcinoma. In: Gass JDM, ed. Stereoscopic atlas of macular diseases: diagnosis and treatment, 4th ed, vol 1. St. Louis: CV Mosby, 1997:236-238.
24. Gass JMD. Acute zonal occult outer retinopathy. Donders lecture: The Netherlands Ophthalmological Society, Maastricht, Holland, June 19, 1992. J Clin Neurol Ophthalmol 1993;13:79-97.
25. Gass JDM, Agarwal AA, Scott IU. Acute zonal occult outer retinopathy: a long-term follow-up study. Am J Ophthalmol 2002;134:329-339.