Cargando…

Ultra-widefield imaging in Takayasu arteritis

Detalles Bibliográficos
Autores principales:	Das, Manmath K, Pokharna, Ridhima, Maikap, Debashis, Panda, Sangram
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/PMC9426060/ https://www.ncbi.nlm.nih.gov/pubmed/35791201 http://dx.doi.org/10.4103/ijo.IJO_528_22

Ejemplares similares

A rare disease with a rarer presentation: Nodular episcleritis in Takayasu’s arteritis
por: Das, Barnita, et al.
Publicado: (2022)

Ultra-widefield imaging in Coats’-type retinitis pigmentosa
por: Jain, Shreyans, et al.
Publicado: (2018)

Nodular scleritis as a presenting feature of Takayasu's arteritis
por: Shukla, Eesha, et al.
Publicado: (2016)

Ultra-widefield angiographic imaging of albumin-bound paclitaxel-induced cystoid macular edema
por: Lee, Junhyuck, et al.
Publicado: (2019)

Utility of multimodal ocular imaging in tuberous sclerosis complex-Review of literature along with a case illustration
por: Venkatesh, Ramesh, et al.
Publicado: (2022)

Multimodal imaging in a case of stellate nonhereditary idiopathic foveomacular retinoschisis
por: Yadav, Divya, 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)

Atypical superior iris and chorioretinal coloboma
por: Parakh, Shweta, et al.
Publicado: (2022)

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

Lady in red: A case of Kearns–Sayre syndrome supported by histopathology
por: Godani, Kanika, 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)

Bilateral Iris depigmentation, transillumination defects and hypotony in Vogt–Koyanagi–Harada disease
por: Garg, Mohit, et al.
Publicado: (2022)

Bilateral orbital Kimura’s disease: A case report and brief review of literature
por: Agrawal, Sahil, et al.
Publicado: (2022)

Relapse of acute lymphoblastic leukemia presenting as masquerade uveitis with hypopyon in a child
por: Rehman, Obaidur, et al.
Publicado: (2022)

Ultra-widefield imaging of golden vitreous membranes requiring pars plana vitrectomy in a case of chronic ocular chalcosis
por: Sundar, M Dheepak, et al.
Publicado: (2019)

An unusual twinning moment – A rare occurrence of unilateral congenital dacryocystocele in a pair of monozygotic identical twins
por: Ramesh, Shruthy V, et al.
Publicado: (2022)

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

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

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

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

Exudative maculopathy in presumed X-linked retinoschisis with review of literature
por: Ramamurthy, Srishti, et al.
Publicado: (2022)

A case of Axenfeld–Rieger syndrome with retinal detachment
por: Chakraborty, Debdulal, et al.
Publicado: (2022)

A rare presentation of ocular histoplasmosis in a patient with systemic nocardiosis
por: Behera, Ranjan K, 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)

Case of probable Vogt–Koyanagi–Harada syndrome: A rare presentation
por: Mehta, Kervi N, 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 rare cause of acquired esotropia: Leprosy
por: Canleblebici, Mehmet, 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)

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

Wolfram syndrome with a rare genetic mutation - Case report
por: Caculo, Divya U, 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)

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

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

Cannot write session to /tmp/vufind_sessions/sess_c7eja2qq0ru4a4dorlc1qigoan