Results 31 to 40 of about 384 (163)

International consensus statement on allergy and rhinology: Allergic rhinitis – 2023

open access: yesInternational Forum of Allergy &Rhinology, Volume 13, Issue 4, Page 293-859, April 2023., 2023
Abstract Background In the 5 years that have passed since the publication of the 2018 International Consensus Statement on Allergy and Rhinology: Allergic Rhinitis (ICAR‐Allergic Rhinitis 2018), the literature has expanded substantially. The ICAR‐Allergic Rhinitis 2023 update presents 144 individual topics on allergic rhinitis (AR), expanded by over 40
Sarah K. Wise   +126 more
wiley   +1 more source

The presentation, clinical features, complications, and treatment of congenital dacryocystocele. [PDF]

open access: yesEye (Lond), 2018
Purpose To determine the incidence and presenting features of congenital dacryocystocele in the United Kingdom. To report on those cases complicated by dacryocystitis, respiratory compromise, and the treatment undertaken.
Davies R   +3 more
europepmc   +2 more sources

Dacryops with extensive lacrimal and maxillary bone defects in four dogs

open access: yesVeterinary Ophthalmology, Volume 24, Issue 2, Page 195-202, March 2021., 2021
Abstract Objective To describe and discuss ventromedial orbital lacrimal gland or duct cysts (dacryops) in dogs with extensive bone defects based on their symptoms, results of diagnostic imaging and histopathological examination, and therapy and discuss their potential origin based on the morphology.
Andrea Steinmetz   +2 more
wiley   +1 more source

An Acquired Dacryocystocele?

open access: yesJournal of Pediatric Ophthalmology & Strabismus, 2021
Tineke, Chan, Sonja, Chen
openaire   +3 more sources

Mini-invasive treatment of a congenital dacryocystocele by means of microdebrider marsupialization in a newborn [PDF]

open access: yes, 2021
Congenital dacryocystocele is a rare clinical condition, more commonly unilateral, secondary to the defective canalization of the nasolacrimal duct. In case of failure of conservative treatment, surgical marsupialization is recommended.
Silvia Osnaghi   +5 more
core   +1 more source

Bilateral mucocele in a patient with Robinow syndrome: A case report

open access: yesIndian Journal of Ophthalmology. Case Reports, 2021
We report the case of a 23-year-old man with Robinow syndrome (RS) and bilateral epiphora due to nasolacrimal duct obstruction associated with bilateral mucoceles.
Gulsah Usta   +5 more
doaj   +1 more source

Idiopathic acquired dacryocystocele in an adult: case report of a rare entity

open access: yesThe Egyptian Journal of Otolaryngology, 2022
Background Idiopathic acquired dacryocystocele in adults is a rare disorder of the lacrimal drainage pathway. Only 20 cases have been reported in the literature. It presents with a triad of epiphora, medial canthal swelling, and recurrent dacryocystitis.
Kirubakaran Kothandaraman   +1 more
doaj   +1 more source

Prenatal diagnosis of congenital head, face, and neck malformations—Is complementary fetal MRI of value?

open access: yesPrenatal Diagnosis, Volume 40, Issue 1, Page 142-150, January 2020., 2020
Abstract Objectives The aim of this study was to evaluate the role of fetal magnetic resonance imaging (MRI) as a complement to ultrasound (US) in the prenatal diagnosis of craniofacial anomalies. Methods A historical cohort study including all pregnant women who were referred for fetal MRI because of antenatal diagnosis of craniofacial anomalies on ...
Roni Zemet   +6 more
wiley   +1 more source

Obstrução nasal num recém-nascido [PDF]

open access: yes, 2021
Dacryocystocele is an uncommon congenital disease affecting less than 1% of newborns. Herein is presented the case of a female newborn with respiratory distress with onset in the first hours of life and worsening during breastfeeding. Resistance to
Neves, João Fonseca   +3 more
core   +1 more source

Home - About - Disclaimer - Privacy