A5012906500- Retinal and Optic Conditions
- Ocular Diseases and Behçet’s Syndrome
- Retinal Diseases and Treatments
- Retinal and Macular Surgery
- Cerebral Venous Sinus Thrombosis
- Retinal Development and Disorders
- Intraocular Surgery and Lenses
- Glaucoma and retinal disorders
- Cardiac Imaging and Diagnostics
- Mitochondrial Function and Pathology
- Ophthalmology and Eye Disorders
- Vasculitis and related conditions
- Ocular Oncology and Treatments
- Vascular Malformations Diagnosis and Treatment
- Airway Management and Intubation Techniques
- Cardiac, Anesthesia and Surgical Outcomes
- Drug-Induced Ocular Toxicity
- Traumatic Ocular and Foreign Body Injuries
- Sarcoidosis and Beryllium Toxicity Research
- Systemic Lupus Erythematosus Research
- Retinoids in leukemia and cellular processes
- Metabolism and Genetic Disorders
- Retinal Imaging and Analysis
- Telomeres, Telomerase, and Senescence
- Complement system in diseases
Associated Retinal Consultants
2016-2025
Beaumont Hospital, Royal Oak
2016-2025
Oakland University
2016-2024
University of Arkansas for Medical Sciences
2024
Rush University Medical Center
2024
Beaumont Health
2023
University of Hawaii System
2020-2022
University of Hawaiʻi at Mānoa
2020-2022
Queen's Medical Center
2021-2022
Rabindranath Tagore Medical College
2021
To describe the features of peripapillary pachychoroid syndrome (PPS), a novel disease spectrum (PDS) entity.Medical records 31 eyes (16 patients) with choroidal thickening associated intraretinal and/or subretinal fluid in nasal macula extending from disk were reviewed (patients PPS). Choroidal thickness was compared 2 age-matched cohorts: typical PDS (17 central serous chorioretinopathy or neovasculopathy) and 19 normal eyes.The patients PPS 81% men aged 71 ± 7 years. Peripapillary...
<h3>Importance</h3> Acute macular neuroretinopathy (AMN) is a rare, yet increasingly recognized, entity identified predominantly in young healthy females with acute onset of paracentral scotomas. The exact pathophysiology unknown but an underlying vascular process suspected. This study used optical coherence tomographic angiography (OCTA) to assess for any evidence flow abnormality the retina or choroid this elusive disease. <h3>Observations</h3> Three eyes from 2 female patients classic...
We report a case of an atypical multifocal choroiditis with retinal vasculitis associated positive West Nile serology. Retrospective report. A healthy 18-year-old man presented floaters in the left eye that started while backpacking Wyoming. Examination and testing revealed numerous chorioretinal lesions eye, as well evidence branch vein occlusion. Serology was for Virus. virus may be trigger development susceptible individuals.
The authors present the first case of paracentral acute middle maculopathy as a manifestation primary antiphospholipid syndrome (APS) with multimodal imaging, including optical coherence tomography angiography (OCTA). association between APS and ophthalmic sequela is well-known. Recent advances in specifically OCTA, allow for better characterization mechanism extent by which retinal arterial thrombosis can cause vision loss. Using advanced imaging modalities, provide comprehensive assessment...
Abstract COVID‐19 has recently been associated with the development of bradyarrhythmias, although its mechanism is still unclear. We aim to summarize existing evidence regarding bradyarrhythmia in and provide future directions for research. Following PRISMA Extension Scoping Reviews, we searched MEDLINE EMBASE all peer‐reviewed articles using keywords including“Bradycardia,” “atrioventricular block,” “COVID‐19″ from their inception October 13, 2021. Forty‐three articles, including 11...
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Purpose: To describe the multimodal imaging findings of posterior polar annular choroidal dystrophy (PPACD). Methods: Retrospective case series 2 patients diagnosed with PPACD. Spectral-domain optical coherence tomography, fundus autofluorescence, and fluorescein angiography PPACD are described. Electroretinography results also presented. Results: Both presented bilateral peripapillary atrophy extending to involve temporal arcades in an annular, foveal sparing pattern. cases demonstrated...
To report a novel presentation of dyskeratosis congenita masquerading as familial exudative vitreoretinopathy.Observational case series involving single family and literature review.A brother sister were diagnosed with vitreoretinopathy at ages 4 2, respectively. Both patients managed laser photocoagulation. Eight years after the initial presentation, both siblings developed pancytopenia secondary to bone marrow failure. Laboratory work-up revealed severely shortened telomere length in...
BACKGROUND AND OBJECTIVE: Punctate inner choroidopathy (PIC) is an inflammatory chorioretinopathy characterized by multiple punctate, hypopigmented fundus lesions. Optical coherence tomography angiography (OCTA) emerging imaging modality that enables high-resolution visualization of the retinal and choroidal vasculature. The objective this study to examine OCTA findings in PIC. PATIENTS METHODS: Observational, retrospective review five patients with RESULTS: revealed several features PIC...
To report the case of a patient who presented with vasculitic central retinal vein occlusion (CRVO), which was result an undiagnosed systemic inflammatory condition, seronegative rheumatoid arthritis (RA). The reduced vision in left eye and polyarthralgia. Fundoscopic examination revealed (CRVO) concurrent evidence vasculitis. Work-up for polyarthralgia included comprehensive serologic testing connective tissue disease, including Vectra® disease activity (DA) testing. Results these studies...