Results 51 to 60 of about 464,407 (196)

Evaluation of Endoscopic Dacryocystorhinostomy Success Rate in Patients with Nasolacrimal Duct Obstruction (2015-18)

مجله دانشگاه علوم پزشکی گرگان, 2022
Background and Objective: Any factor that disrupts the tear duct can cause epiphora, one of the most prevalent causes for patients to go to ophthalmology clinics. Nasolacrimal duct obstruction can be congenital or acquired.
Masoumeh Eslami, Fatemeh Abdi, Marjan Akbari-Kamrani, Arzhang Gordiz, Fatemeh Najafi   +4 more
doaj  

Bilateral congenital lacrimal fistulas in an adult as part of ectrodactyly-ectodermal dysplasia-clefting syndrome: A rare anomaly

Indian Journal of Ophthalmology, 2015
Ectrodactyly-ectodermal dysplasia and clefting syndrome or "Lobster claw" deformity is a rare congenital anomaly that affects tissues of ectodermal and mesodermal origin.
Debangshu Ghosh, Somnath Saha, Sumit Kumar Basu   +2 more
doaj   +1 more source

Nance‐Horan Syndrome: Further Delineation of the Affected Male and the Female Carrier Phenotypes

American Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 642-652, March 2026.
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, Chad R. Haldeman‐Englert, Marja Hietala, Melisa S. Tanverdi, Patrick P. Koty, Diana Brightman, Eniolami Dosunmu, Shailja Tibrewal, Savleen Kaur, Anupriya Kaur, Raj Kumar Verma, Alejandra G. de Alba Campomanes, Virginia Utz, Anne M. Slavotinek, Cynthia Curry   +14 more
wiley   +1 more source

A rare cause of nasolacrimal duct obstruction: Dentigerous cyst in the maxillary sinus

Indian Journal of Ophthalmology, 2009
The most common abnormality of the lacrimal drainage system is congenital or acquired nasolacrimal duct obstruction. The causes of acquired nasolacrimal duct obstruction may be primary or secondary.
Ray Biswarup, Bandyopadhyay Saumendra, Das Debabrata, Adhikary Bivas   +3 more
doaj  

Non‐RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome

American Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 661-672, March 2026.
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, Alexsandra Christianne Malaquias, Debora Romeo Bertola, Raissa Carneiro Rezende, Laurana De Polli Cellin, Lucas Vieira Lacerda Pires, Ana Maria Santillan‐Vasconez, Antônio Marcondes Lerario, Renata da Cunha Scalco, Alexander Augusto de Lima Jorge   +9 more
wiley   +1 more source

Microbiology and Antibiotic Susceptibility Pattern in Congenital Nasolacrimal Duct Obstruction

Delhi Journal of Ophthalmology
Purpose: To analyze the microbiological spectrum and antibiotic sensitivity in children with congenital nasolacrimal duct obstruction (CNLDO) and determine the empirical drug of choice.
Maneksha Velu, K. S. Aparna
doaj   +1 more source

Ophthalmic Manifestations in A Patient With Kabuki Syndrome: A Case Report With a KDM6A Gene Variant

Case Reports in Ophthalmological Medicine, Volume 2026, Issue 1, 2026.
Kabuki syndrome (KS) is a rare genetic disorder with a wide phenotypic spectrum and several genotypic variants. KS can result from mutations on Chromosome 12 (KMT2D gene) and Chromosome X (KDM6A gene). The KDM6A gene mutation is seen in approximately 2%–6% of Kabuki syndrome cases.
Tülin Öğreden, Gülçiçek Cayhan, Semonti Nandi   +2 more
wiley   +1 more source

Endoscopic dacryocystorhinostomy to treat congenital nasolacrimal canal dysplasia: a retrospective analysis in 40 children

BMC Ophthalmology, 2019
Background To investigate the therapeutic effectiveness and safety of endoscopic dacryocystorhinostomy (EN-DCR) to treat congenital nasolacrimal canal dysplasia (CNCD). Methods Forty children (50 eyes) with congenital nasolacrimal duct obstruction (CNLDO)
Yan-Hui Cui, Cheng-Yue Zhang, Wen Liu, Qian Wu, Gang Yu, Li Li, Wen-Bin Wei   +6 more
doaj   +1 more source

Conventional or Endoscopic Probing for Congenital Nasolacrimal Duct Obstruction

, 2001
PurposeTo compare conventional and endoscopic probing for congenital nasolacrimal duct obstruction in infants.MethodsConventional probing was performed in 22 eyes of 18 patients, age range 7–14 months (mean 11.4 months).
M. Orhan, M. Önerci, M. Írkeç, P. Çal   +3 more
core   +1 more source

Pyriform Plasty as an Adjunct to Septoplasty: A Double‐Blind Randomized Trial in Patients With Septal Deviation

Laryngoscope Investigative Otolaryngology, Volume 10, Issue 6, December 2025.
ABSTRACT Introduction The study was designed to compare the final long‐term outcomes of septoplasty with and without unilateral pyriform plasty on the concave side in patients with septal deviation. Materials and Methods A randomized clinical trial was conducted from 2020 to 2023. Patients were randomly divided into two groups of 30.
Matin Ghazizadeh, Behrouz Barati, Mohammad Moini, Homeira Mansurzadeh   +3 more
wiley   +1 more source