Results 31 to 40 of about 1,130 (139)
Children with congenital glaucoma are often accompanied by acquired epiblepharon in the lower eyelid, which causes entropion of the lower eyelid and damages the cornea.To infer the possible causes of lower eyelid entropion by comparing the difference of ocular axis and corneal diameter between inverted and non-inverted ciliary eyes in children with ...
Wang, Yue +5 more
openaire +2 more sources
Abstract Purpose To describe the use of coronofrontal rhytidectomy (CFR) for the treatment of severe pseudoptosis and superior entropion in dogs, and to provide guidelines for the selection of surgical technique depending on presentation. Methods A review of medical records of dogs that underwent rhytidectomy from 2002 to 2023 was carried out ...
Rita Vilao Cardoso +5 more
wiley +1 more source
European S2k guidelines on management of autoimmune blistering diseases in children and adolescents
Autoimmune blistering disorders (AIBDs) in children are rare, challenging to diagnose and treat and often require immunosuppressants. Until now, no paediatric care guidelines existed. The EADV Task Force for AIBDs has developed the consensus‐based recommendations, enabling physicians to adopt a uniform, tailored treatment strategy to improve outcomes ...
A. Nanda +31 more
wiley +1 more source
ABSTRACT Objective To identify commonly presented dog breeds and potentially heritable ophthalmic diseases encountered by veterinarians practicing ophthalmology in Japan. Methods A survey was distributed through the Japanese Society of Comparative and Veterinary Ophthalmology.
Victoria Caballero +8 more
wiley +1 more source
ABSTRACT Genetic disorders commonly share features such as developmental delays, cognitive impairment, and behavioral challenges, yet many conditions also present unique dysmorphic features that distinguish them. Performing a thorough medical and family history and a detailed physical exam with attention to dysmorphic features is often the first step ...
Natasha L. Rudy +15 more
wiley +1 more source
Abstract Homozygous sauteur d'Alfort rabbits have a splicing‐site mutation in the RAR‐related orphan receptor B (RORB) gene that causes changes in their locomotion. These rabbits sometimes walk on their thoracic limbs, especially at higher speeds. They also experience additional abnormalities, including eye alterations such as blindness due to retinal ...
Kerstin Müller +4 more
wiley +1 more source
Surgical Treatment of Epibulbar Malformations
Aim. Analysis of the results of surgical treatment in patients with epibulbar malformations. Patients and Methods. The study included 126 patients with a preliminary diagnosis of “epibulbar neoplasm”, who received treatment from January 2013 to December ...
S. V. Saakyan +4 more
doaj +1 more source
A Japanese Case of Lenz‐Majewski Syndrome With a Novel PTDSS1 Variant
A Japanese girl with a de novo PTDSS1 R95Q variant showed mild sclerosing bone dysplasia. Functional and structural analyses revealed intermediate PS synthesis activity compared to previously reported variants, suggesting a broader phenotypic spectrum of LMS.
Yasuko Kobari +8 more
wiley +1 more source
Use of sodium hyaluronate subdermal injection for treatment of upper eyelid entropion in a rabbit
Abstract A 2‐year‐9‐month‐old, male, neutered, Dutch rabbit was diagnosed with bilateral epiphora, upper eyelid entropion, secondary trichiasis and superficial corneal ulceration. Corneal healing was delayed until temporary upper eyelid eversion with Histoacryl®. Once this dissolved, entropion and corneal ulceration re‐occurred.
Catarina Alexandra Ventura Goncalves +2 more
wiley +1 more source
Abstract The objective was to evaluate the progression and management of eyelid tacking sutures before permanent eyelid surgical correction. A 1‐year‐old Aberdeen black Angus bull presented with a 1‐month history of bilateral corneal ulcers. Ophthalmic examination revealed an infected stromal corneal ulcer on the left eye and bilateral lower eyelid ...
Leila Bedos +4 more
wiley +1 more source

