Results 61 to 70 of about 4,922 (188)

Monitoring and management of congenital entropion in lambs:A prospective study

open access: yes, 2013
This prospective study investigated the prevalence, the ocular features and the impact on zootechnic performance of congenital entropion in a sheep flock. A total of 318 Ile de France and Texel purebred and crossbred lambs were observed from birth to the
Muylkens, B.   +4 more
core   +1 more source

Procédure de Quickert dans le traitement de l’entropion sénile de la paupière inférieure

open access: yesJournal de la Société Marocaine d’Ophtalmologie, 2018
L’entropion est une malposition palpébrale correspondant au retournement du bord libre de la paupière vers le globe oculaire. L’entropion sénile représente une forme clinique dont le mécanisme est plurifactoriel.
S. cherkaoui   +5 more
doaj   +1 more source

Comparison of entropion outcome with and without intervention in Romane and Ile de France sheep breeds

open access: yesVeterinary Medicine and Science
Background Congenital entropion is the most frequent ocular disorder in newborn lambs of certain sheep breeds, which, if not treated, can result in complete blindness and death due to starvation.
Hossein Esmaeili   +7 more
doaj   +1 more source

Stades method for surgical correction of upper eyelid trichiasis-entropion: results and follow-up in 21 cases Método de Stades para a correção da triquíase-entrópio da pálpebra superior: resultados e acompanhamento de 21 casos

open access: yesCiência Rural, 2000
Trichiasis is a condition in which lhe cuia and facial hairs grow toward lhe córnea or the conjunctiva. The hairs arising from normal sites are pointed aí an abnormal direction.
José Luiz Laus   +4 more
doaj   +1 more source

The spontaneous development of entropion in a laboratory cat

open access: yes, 2013
An 11-month old, intact male domestic short-haired cat presented to the Cornell University Center for Animal Resources and Education (CARE) laboratory animal veterinarians on January 18, 2013 for complaints by the animal husbandry staff of severe ...
Peneyra, Samantha M.
core   +4 more sources

Lower lid entropion secondary to treatment with alpha-1a receptor antagonist: a case report

open access: yesJournal of Medical Case Reports, 2010
Introduction The use of alpha-1a receptor antagonists (tamsulosin) is widely accepted in the treatment of benign prostatic hypertrophy (BPH). It has previously been implicated as a causative agent in intra-operative floppy iris syndrome due to its ...
Simcock Peter, Waqar Salman
doaj   +1 more source

Clamp-assisted retractor advancement for lower eyelid involutional entropion [PDF]

open access: yes, 2013
PURPOSE: To describe a novel approach to internal repair of lower lid entropion using the Putterman clamp. METHODS: Retrospective, consecutive case series of patients with entropion who underwent retractor advancement using the clamp. RESULTS: Seven eyes
Fung, NSK, Marcet, MM
core  

Frequency of Eyelid Malpositions and their Treatment Results in Patients Referred to Ophthalmology Clinics in Educational Yazd Hospitals

open access: yesMajallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Shahīd Ṣadūqī Yazd, 2012
Introduction: Entropion and ectropion with involutional changes are the most common eyelid malpositions. Entropion is a condition in which the eyelid margin turns inwards against the globe and ectropion is a malposition in which the lid turns outwards or
M Rafieian   +3 more
doaj  

Surgical outcome of involutional lower eyelid entropion correction using transcutaneous everting sutures in Chinese patients

open access: yes, 2014
To evaluate the clinical efficacy of transcutaneous everting sutures for lower eyelid involutional entropion in Chinese patients. A retrospective, non-comparative, interventional case series.
Yuen, CY   +4 more
core   +1 more source

Exposure, entropion, and bilateral corneal ulceration in a newborn as a manifestation of chromosome 22 q11.2 duplication syndrome

open access: yesAmerican Journal of Ophthalmology Case Reports, 2019
Purpose: Chromosome 22q11.2 micro-duplication syndrome (MDS), is a rare autosomal dominant condition, with a highly variable phenotype that ranges from unremarkable and asymptomatic, to fatal due to cardiovascular defects.
Hamid-Reza Moein   +8 more
doaj   +1 more source

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