Cargando…

A case of Axenfeld–Rieger syndrome with retinal detachment

Detalles Bibliográficos
Autores principales:	Chakraborty, Debdulal, Basak, Samar K, Saha, Asmita, Mondal, Soumen, Mitra, Arijit
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer - Medknow 2022
Materias:	Rare Eye Diseases, Photo Essay
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9426138/ https://www.ncbi.nlm.nih.gov/pubmed/35791188 http://dx.doi.org/10.4103/ijo.IJO_2737_21

Ejemplares similares

Complete detachment of the Schwalbe’s line in a case of Axenfeld-Reiger anomaly - A rare presentation
por: Mitra, Arijit, et al.
Publicado: (2022)

A rare case of unilateral Axenfeld–Rieger anomaly associated with optic disc coloboma: A multimodal imaging canvas
por: Ramesh, Prasanna V, et al.
Publicado: (2022)

Double trouble: Microspherophakia with Axenfeld-Rieger anomaly
por: Shakrawal, Jyoti, et al.
Publicado: (2019)

Bacillary layer detachment in a patient with serpiginoid choroiditis
por: Rodríguez-Vidal, Cristina, et al.
Publicado: (2022)

Spontaneous resolution of Descemet’s membrane detachment following bleb needling in a patient with iridocorneal endothelial syndrome: A case report
por: Maheshwari, Devendra, et al.
Publicado: (2022)

Bilateral central retinal artery occlusion: Endovenous and intra-arterial thrombolysis in a patient with a subsequent diagnosis of antiphospholipid antibody syndrome
por: Pérez, Sara M P, et al.
Publicado: (2022)

A case of central retinal artery occlusion due to atrial myxoma with excellent visual recovery
por: Balasubramaniam, Santosh, et al.
Publicado: (2022)

Optical coherence tomography: Angiography visualization of retinal oxalosis in primary hyperoxaluria, a case report
por: Barigali, A, et al.
Publicado: (2022)

Effect of combined laser and anti-vascular endothelial growth factor in a retinal capillary macroaneurysm
por: Nadig, Ramya R, et al.
Publicado: (2022)

Utility of multimodal imaging in the detection and follow-up of retinal astrocytic hamartomas in a young girl with tuberous sclerosis complex
por: Chandran, Kiran, et al.
Publicado: (2022)

Swept source optical coherence tomography angiography of a case of retinal artery macro-aneurysm before and after combined laser and intra-vitreal ranibizumab treatment
por: Brar, Manpreet, et al.
Publicado: (2022)

Waardenburg Syndrome Type 1
por: Agrawal, Rakshit, et al.
Publicado: (2022)

Electron microscopy in Cogan–Reese syndrome
por: Behera, Geeta, et al.
Publicado: (2022)

Beyond retina in Sjogren–Larsson syndrome
por: Pawar, Neelam, et al.
Publicado: (2022)

Inverse Duane’s retraction syndrome – A case report
por: Murthy, Sowmya Raveendra, et al.
Publicado: (2022)

Wolfram syndrome with a rare genetic mutation - Case report
por: Caculo, Divya U, et al.
Publicado: (2022)

Ocular presentation of Walker–Warburg syndrome with POM2 mutation
por: Sukhija, Jaspreet, et al.
Publicado: (2022)

Case of probable Vogt–Koyanagi–Harada syndrome: A rare presentation
por: Mehta, Kervi N, et al.
Publicado: (2022)

Lady in red: A case of Kearns–Sayre syndrome supported by histopathology
por: Godani, Kanika, et al.
Publicado: (2022)

Hypertensive retinopathy in a young patient! Don’t forget Alport syndrome
por: Agrawal, Nikhil, et al.
Publicado: (2022)

A rare case of congenital fibrosis of extra ocular muscles with Kallmann syndrome
por: Yenugandula, Raman, et al.
Publicado: (2022)

Exotropia in a case of Ellis Van Creveld syndrome: A rare case report
por: Nayak, Swatishree, et al.
Publicado: (2022)

Ankyloblepharon-ectodermal dysplasia-clefting syndrome: Surgical and medical management in an infant with bilateral corneal perforations
por: Hossain, Ruhella R, et al.
Publicado: (2022)

A new entity of hypomyelination with atrophy of basal ganglia and cerebellum-like syndrome with bilateral developmental cataract
por: De Piedade Sequeira, Linda Maria Genoveva, et al.
Publicado: (2022)

Optical coherence tomography and angiography features of pigmented ocular fundus lesions in hereditary colonic polyposis syndrome
por: Sagar, Pradeep, et al.
Publicado: (2022)

Novel NR2F1 variant identified by whole-exome sequencing in a patient with Bosch–Boonstra–Schaaf optic atrophy syndrome
por: Kocaaga, Ayca, et al.
Publicado: (2022)

Pseudoproptosis in a case of familial hereditary cerebellar ataxia
por: Nivean, Pratheeba D, et al.
Publicado: (2022)

Keratoconus associated with hereditary sensory and autonomic neuropathy II
por: Shah, Zalak, et al.
Publicado: (2022)

Optic nerve demyelination as the presenting feature of adrenoleukodystrophy in a child
por: Kasturi, Nirupama, et al.
Publicado: (2022)

Congenital entropion with progeria: 4 going 40
por: Gupta, Himika, et al.
Publicado: (2022)

Eye signs in a child with ROBO3 gene mutation
por: Yoganathan, Sangeetha, et al.
Publicado: (2022)

A rare presentation of ocular histoplasmosis in a patient with systemic nocardiosis
por: Behera, Ranjan K, et al.
Publicado: (2022)

A rare cause of acquired esotropia: Leprosy
por: Canleblebici, Mehmet, et al.
Publicado: (2022)

Ultra-widefield imaging in Takayasu arteritis
por: Das, Manmath K, et al.
Publicado: (2022)

Importance of adherence to topical cysteamine in infantile ocular cystinosis: An illustrative case
por: Bayram-Suverza, Mauricio, et al.
Publicado: (2022)

Polymerase chain reaction: A novel way to detect ocular dirofilariasis
por: Pradhan, Arkaprava, et al.
Publicado: (2022)

Bilateral buphthalmos with congenital cataract in a floppy infant
por: Jacob, Ninan, et al.
Publicado: (2022)

A rare case of congenital aniridia with an unusual run-on mutation in PAX6 gene
por: Ratna, Ria, et al.
Publicado: (2022)

Angle-closure glaucoma associated with autosomal recessive bestrophinopathy
por: Raja, Vidya, et al.
Publicado: (2022)

Anterior scleritis in pemphigus vulgaris: A rare ocular manifestation
por: Bhole, Pradnya K, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_e5nc78kdhmnvbth21ih8u09moo