Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Dhariana, Acon"'
Peters plus syndrome and Chorioretinal findings associated with B3GLCT gene mutation - a case report
Publikováno v:
BMC Ophthalmology, Vol 20, Iss 1, Pp 1-4 (2020)
Abstract Background Peters plus syndrome (PPS) is a combination of congenital Peters anomaly and systemic abnormalities. It is inherited most commonly in an autosomal recessive pattern with homozygous B3GLCT mutations. Ocular findings consist predomi
Externí odkaz:
https://doaj.org/article/10f956925dc94484be2003ab2440c777
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 23, Iss , Pp 101177- (2021)
Purpose: To illustrate the spectrum of clinical and imaging features in patients with unilateral Coats’ disease at baseline and in response to treatment with laser, intravitreal bevacizumab, and regional steroids. Observations: Telangiectasias, mac
Externí odkaz:
https://doaj.org/article/c199a68781fc498d871fd4bdd4596d67
Publikováno v:
Taiwan Journal of Ophthalmology, Vol 11, Iss 2, Pp 187-189 (2021)
The aim of the study was to describe the ocular findings following an accidental high-voltage electrical discharge. A 32-year-old male suffered an accidental electric discharge of 10,000 volts of direct current. He developed cortical, nuclear, and po
Externí odkaz:
https://doaj.org/article/b4c1ab4156ea4553b739cc68375d40d1
Autor:
Jose J. Echegaray, Prashanth Iyer, Dhariana Acon, Catherin Negron, Sophia El Hamichi, Audina M. Berrocal
Publikováno v:
Journal of VitreoRetinal Diseases. 7:79-82
Purpose: To report OCTA findings in a case of nonaccidental injury (NAI). Methods: Retrospective review of a clinical case. Results: A 5-year-old White child with a history of NAI at age 1 year presented with reduced vision in the left eye resulting
Publikováno v:
Journal of VitreoRetinal Diseases. 6:452-456
Purpose: This work describes a unique clinical feature in Coats disease. Methods: A retrospective series of 2 cases is reported. Results: Two pediatric patients receiving treatment for Coats disease were included. In both cases, vision worsened secon
Autor:
Sophia El Hamichi, Dhariana Acon, Veronica Kon Graversen, Aaron S. Gold, Audina M. Berrocal, Timothy G. Murray
Publikováno v:
Journal of Ophthalmology, Vol 2020 (2020)
Introduction. Retinoblastoma (RB) is the most common eye tumor in children. There have been significant improvements in treatment options targeting killing the tumor while also conserving the eye and attempting to conserve functional vision. Retinal
Externí odkaz:
https://doaj.org/article/213e6a1d5ab840fdbfd0f91097f86e1d
Publikováno v:
The Pan-American Journal of Ophthalmology, Vol 3, Iss 1, Pp 18-18 (2021)
Purpose: To report the demand of ophthalmic services and the prevalence of the main ophthalmic pathologies in a rural population of Costa Rica. Study Design: A cross-sectional study of all individuals seen at the ophthalmology outpatient clinic durin
Externí odkaz:
https://doaj.org/article/d4ab907b75ed4b7aa74934c7ccfaeb30
Autor:
Roberto Gallego-Pinazo, J.F. Arevalo, Sergio Rojas, Jay Chhablani, Marcelo Zas, Maria H. Berrocal, Dhariana Acon, Rosa Dolz-Marco, Mauricio Maia, Lihteh Wu, Jose A. Roca
Publikováno v:
International Ophthalmology. 42:951-958
The purpose of this study was to report the 5-year outcomes of treatment-naive eyes with cystoid macular edema secondary to central retinal vein occlusion treated with intravitreal bevacizumab in routine clinical practice. We conducted multicenter re
Autor:
Dhariana Acon, Audina M. Berrocal, Noemi Güemes-Villahoz, Sophia El Hamichi, Rebecca Tanenbaum
Publikováno v:
Ophthalmic Surgery, Lasers and Imaging Retina. 52:155-159
Familial exudative vitreoretinopathy (FEVR) is a rare inherited disorder affecting retinal angiogenesis that may present with a wide range of phenotypic characteristics. In this report, the authors describe an atypical presentation of FEVR in a healt
Publikováno v:
Case Reports in Ophthalmology
Case Reports in Ophthalmology, Vol 11, Iss 3, Pp 612-619 (2020)
Case Reports in Ophthalmology, Vol 11, Iss 3, Pp 612-619 (2020)
Optic disc coloboma (ODC) is a rare congenital anomaly of the optic nerve. Optical coherence tomography (OCT) helps to monitor the complications when there is associated retinoschisis, retinal detachment, or peripapillary neovascularization, while be