Results 21 to 30 of about 1,144,867 (168)

Application of ultrasound biomicro-scopy in the planning of cataract surgery in anterior megalophthalmos

Indian Journal of Ophthalmology, 2011
Anterior megalophthalmos, a rare hereditary disorder, is macrocornea (horizontal corneal diameter more than 13 mm) in association with enlarged lens-iris diaphragm and ciliary ring.
Mohammad Ali Zare, Bahram Eshraghi, Mohammad Yaser Kiarudi, Ebrahim Azaripour Masoule   +3 more
doaj   +1 more source

Bilateral hypopyon uveitis in carcinoma of breast: Masquerade syndrome and review of literature

Indian Journal of Ophthalmology. Case Reports, 2023
Maquerade syndromes are a group of ocular diseases that mimic inflammation but are due to neoplastic or less commonly non- neoplastic diseases. Metastatic choroidal disease is the most frequent clinical feature in carcinoma breast.
Radha Annamalai, Priya Delampady, Jyotirmay Biswas   +2 more
doaj   +1 more source

Delayed inflammation associated with retained perfluorocarbon liquid

Indian Journal of Ophthalmology, 2011
A 55-year-old woman, with history of cataract surgery 1 year back, presented with features of ocular inflammation for last 3 months. She had no history of any other intraocular surgery.
S Pradeep, Jay K Chhablani, Bhavin Patel, Padmaja Rani   +3 more
doaj   +1 more source

Unusual initial manifestation of choroidal melanoma in a 46-year-old adult with rapid growth over 9 months

American Journal of Ophthalmology Case Reports, 2022
Purpose: To report a case with unusual initial manifestation of uveal melanoma in a 46-year-old adult. Observations: A 46-year-old man demonstrated a mid-peripheral temporal partially hyperpigmented lesion in his left eye.
Olga Furashova, Katrin Engelmann, Antonia M. Joussen, Aline I. Riechardt   +3 more
doaj   +1 more source

Progressive Supranuclear Palsy in India: Insights from a Large Multicenter Clinical Cohort (Project PAIR‐PSP)

Movement Disorders Clinical Practice, EarlyView.
Background Progressive supranuclear palsy (PSP) is a rare and devastating tauopathy with limited global data. Given India's large population, genetic diversity, and clinical heterogeneity, large multicenter datasets are crucial to enrich global understanding of PSP. Objective To characterize the demographic, clinical, and phenotypic profiles of a large
Prashanth Lingappa Kukkle, Divyani Garg, Jacky Ganguly, Soaham Desai, Rukmini Mridula Kandadai, Sahil Mehta, Pettarusp Murzban Wadia, Deepika Joshi, Lulup Sahoo, Vijayashankar Paramanandam, Taallapalli Ashok Vardhan Reddy, Adreesh Mukherjee, Syam Krishnan, Kuldeep Shetty, Charulata Sankhla, Pankaj Agarwal, Heli S. Shah, Suvorit Bhowmick, Mitesh Chandarana, Malini Venkata, Thenral S. Geetha, Ramesh Menon, Sandeep Charugulla, Sakthivel Murugan, Ravi Gupta, Niraj Kumar, Atanu Biswas, Hrishikesh Kumar, Rupam Borgohain, Huw Morris, Vedam. L Ramprasad, Parkinson's Research Alliance of India (PRAI) and the Global Parkinson's Genetic Program (GP2)   +31 more
wiley   +1 more source

Late occurrence of granular dystrophy in bilateral keratoconus: Penetrating keratoplasty and long-term follow-up

Indian Journal of Ophthalmology, 2011
We report a rare case of keratoconus with granular dystrophy with a follow-up of two decades, documenting the sequential presentation of two diseases confirmed by histology and genetic studies.
Varsha M Rathi, Geeta K Vemuganti, Virender S Sangwan, Chitra Kannabiran   +3 more
doaj   +1 more source

Who Can Afford to Fail? Investigating Science Students' Perceptions of Failure Through the Lens of Their Identities

Science Education, EarlyView.
ABSTRACT Scientists agree that learning to cope with failures is an important skill for science students to develop, and students who participate in science research often have positive outcomes after coping with science failures. However, the experience of failure in undergraduate science education more broadly seems to have an overall negative impact
Sandhya Krishnan, Isobel D. Cobb, Joseph A. Harsh, Manuela Mejia, Lisa Corwin   +4 more
wiley   +1 more source

Masquerade syndrome in ocular surface squamous neoplasia

, 2022
The aim of this study was to alert the ophthalmic community to an atypical manifestation of ocular surface squamous neoplasia, which may delay diagnosis and treatment and result in a guarded visual prognosis and significant sequelae.
Dalton de Freitas Santoro (12684689), Laura Caldas dos Santos (12684686), Raysa Victoria de Oliveira Cechim (12684683), Denise de Freitas (4894147), Luiz Antônio Vieira (12684692), Luciene Barbosa de Sousa (4958035)   +5 more
core   +1 more source

A seemingly usual case of paraplegia with MRI diagnosis of meningioma: An unexpected course of events leading to inflammatory necrotizing myelopathy

Indian Spine Journal, 2021
Necrotizing myelopathy is a rare but potentially devastating disease and an important cause of paralysis. Its diagnosis can be challenging inspite of availability of magnetic resonance imaging (MRI) and laboratory investigations.
Punit Tiwari, Harmeet Kaur, Gaurav Sharma   +2 more
doaj   +1 more source

Giant cellulitis-like Sweet syndrome: An underrecognized clinical variant mimicking skin and soft tissue infection

IDCases, 2020
A new clinical variant of Sweet syndrome, called giant cellulitis-like Sweet syndrome, can masquerade as cellulitis because the patients present with an acute onset of large erythematous plaques, fever, and leukocytosis with neutrophil predominance. This
Hayato Mitaka, Rita Jammal, Joseph Saabiye, Stanley Yancovitz, David C. Perlman   +4 more
doaj   +1 more source