Electrooculography and optical coherence tomography reveal late-onset best disease

被引:2
作者
机构
[1] Nova Southeastern University, Tampa, FL
来源
Makati, Ravie (RM1051@nova.edu) | 1600年 / Lippincott Williams and Wilkins卷 / 91期
关键词
adult-onset foveomacular dystrophy; Best; Best disease; bestrophin; pattern dystrophy of the RPE; retinal dystrophy;
D O I
10.1097/OPX.0000000000000403
中图分类号
学科分类号
摘要
Purpose. Best vitelliform macular dystrophy, also known as Best disease, is a macular dystrophy characterized by bilateral yellowish egg yolkYlike lesion(s) present within the maculae. It is a slowly progressive disease that usually presents at childhood. Best vitelliform macular dystrophy frequently proceeds through stages, beginning with a classic presentation described as vitelliform. A similar condition, known as adult-onset foveomacular vitelliform dystrophy, has been described among adult patients. Although the two maculopathies may look similar, they are considered two separate entities, because of the age of onset and overall clinical presentation. Case Report. A 54-year-old man presented with gradual-onset blurred near vision in each eye. Previous records showed a history of unremarkable dilated fundus examinations for the past 8 years. Best-corrected distance acuities measured 20/20 OD and 20/20 OS. Amsler grid testing revealed a mild metamorphopsia OD and OS. Dilated fundoscopy revealed macular pseudohypopyon in each eye. In vivo imaging of the maculae was obtained with spectral-domain optical coherence tomography findings. Electrooculography findings were consistent with Best vitelliform macular dystrophy of atypical, late onset. Conclusions. Best vitelliform macular dystrophy may vary in its presentation. Electrooculography and spectral-domain optical coherence tomography can aid in establishing the definitive diagnosis. © 2014 American Academy of Optometry.
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页码:e274 / e277
页数:3
相关论文
共 9 条
[1]  
MacDonald I.M., Lee T., Updated 2013 Accessed August 25, 2014, GeneReviewsi: Best Vitelliform Macular Dystrophy, (1993)
[2]  
Sodi A., Passerini I., Murro V., Caputo R., Baccigm BodojM., Torricelli F., Menchini U., BEST1 sequence variants in Italian patients with vitelliform macular dystrophy, Mol Vis, 18, pp. 2736-2748, (2012)
[3]  
Finger R.P., Charbel Issa P., Kellner U., Schmitz-Valckenberg S., Fleckenstein M., Scholl H.P., Holz F.G., Spectral domain optical coherence tomography in adult-onset vitelliform macular dystrophy with cuticular drusen, Retina, 30, pp. 1455-1464, (2010)
[4]  
Kanski J.J., Clinical Ophthalmology: A Systematic Approach, (2007)
[5]  
Seddon J.M., Afshari M.A., Sharma S., Bernstein P.S., Chong S., Hutchinson A., Petrukhin K., Allikmets R., Assessment ofmutations in the Bestmacular dystrophy (VMD2) gene in patients with adult-onset foveomacular vitelliform dystrophy, age-related maculopathy, and bull's-eye maculopathy, Ophthalmology, 108, pp. 2060-2067, (2001)
[6]  
Cohn A.C., Turnbull C., Ruddle J.B., Guymer R.H., Kearns L.S., Staffieri S., Daggett H.T., Hewitt A.W., MacKey D.A., Best's macular dystrophy in Australia: Phenotypic profile and identification of novel BEST1 mutations, Eye (Lond), 25, pp. 208-217, (2011)
[7]  
Jarc-Vidmar M., Kraut A., Hawlina M., Fundus autofluorescence imaging in Best's vitelliform dystrophy, Klin Monbl Augenheilkd, 220, pp. 861-867, (2003)
[8]  
Gass J.D.M., Stereoscopic Atlas of Macular Diseases: Diagnosis and Treatment, 4th Ed. St. Louis, MO Mosby, (1997)
[9]  
Epstein G.A., Rabb M.F., Adult vitelliform macular degeneration: Diagnosis and natural history, Br J Ophthalmol, 64, pp. 733-740, (1980)