Results 81 to 90 of about 5,174 (217)
Transpalpebral enucleation for an irreparable ocular injury in an ox. Clinical presentation of the damaged right eye. Preparation of the site, Peterson nerve block, and temporary tarsorrhaphy. Circumferential elliptical skin incision and excision of the damaged eye (enucleation). Orbital packing followed by interlocking silk sutures.
Getachew Tadesse
wiley +1 more source
ABSTRACT Background and Aims Standard management of dry eye disease (DED) relies on artificial tears, anti‐inflammatory therapy, and punctal occlusion in selected cases. However, some patients continue to report persistent symptoms. The present article reviewed the efficacy of Botulinum Toxin A (BTX‐A) for DED that remained symptomatic after these ...
Mirsaeed Abdollahi +6 more
wiley +1 more source
Nance‐Horan Syndrome: Further Delineation of the Affected Male and the Female Carrier Phenotypes
ABSTRACT Nance‐Horan syndrome (NHS; OMIM 302350) is a rare, X‐linked syndrome characterized by bilateral congenital cataracts leading to profound vision loss, specific dental anomalies including characteristic screwdriver blade‐shaped incisors, facial anomalies, and intellectual disability.
Maria K. Haanpää +14 more
wiley +1 more source
Probing of the Nasolacrimal Duct
Congenital nasolacrimal duct obstructions may present with mucoid discharge, epiphora, or lacrimal swelling, and is most commonly located at the distal end of the nasolacrimal duct. Nasolacrimal duct probing may be performed to treat an obstruction after
Blessing, Nathan +5 more
core +1 more source
Primary non Hodgkin's lymphoma of the lacrimal sac is uncommon but potentially delay in diagnosis as it may mimic the presentation of primary post saccal nasolacrimal duct obstruction. In this article, we reported a case of primary non Hodgkin's lymphoma
Noor Shirlyna Irma Ngah +3 more
doaj +1 more source
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim +9 more
wiley +1 more source
Purpose: Lacrimal probing is the treatment of choice for congenital nasolacrimal duct obstruction that does not have a spontaneous resolution; however, there is no consensus about the best time for probing and if it is superior to other therapies.
El Dib, Regina [UNESP] +5 more
core +1 more source
Kanograt Pornpanich,1 Panitee Luemsamran,1 Amornrut Leelaporn,2 Jiraporn Santisuk,3 Nattaporn Tesavibul,1 Buntitar Lertsuwanroj,1 Sumalee Vangveeravong1 1Department of Ophthalmology, 2Department of Microbiology, 3Eye Surgery Unit, Faculty of Medicine ...
Vangveeravong S +6 more
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Pseudodacryocystitis and nasolacrimal duct obstruction secondary to ethmoiditis
A 23-year-old woman presented with clinical symptoms suggestive of acute dacryocystitis. She had no history of epiphora, and her lacrimal drainage system was patent on irrigation.
core +1 more source
Unilateral congenital nasolacrimal duct obstruction and amblyopia risk factors
Akshay Badakere, Tabita Naomi Veeravalli, Sadiya Iram, Milind N Naik, Mohammad Javed Ali Govindram Seksaria Institute of Dacryology, L.V. Prasad Eye Institute, Hyderabad, India Introduction: This study aimed to investigate the prevalence of amblyopia ...
Badakere A +4 more
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