Results 51 to 60 of about 1,996 (198)

Amblyopia Risk Factors in Newborns With Congenital Nasolacrimal Duct Obstruction

, 2020
To investigate the presence of amblyopia risk factors in newborns with congenital nasolacrimal duct obstruction (CNLDO) and age-matched healthy control ...
Michele Iester, Aldo Vagge, Vagge, Aldo, Marco Pellegrini, Carlo Enrico Traverso, Tulumello, Claudia, Claudia Tulumello, Iester, Michele, Marco Di Maita, Pellegrini, Marco, Di Maita, Marco, Traverso, Carlo Enrico   +11 more
core   +1 more source

Outcome of probing and syringing in congenital nasolacrimal duct obstruction at various age groups in a tertiary eye center in Western Nepal

Asian Journal of Medical Sciences, 2018
Background: Congenital nasolacrimal duct obstruction (CNLDO) is one of the commonest problems encountered in daily ophthalmology practice. Though probing and syringing is the mainstay of management of CNLDO, there is no clear guideline about the optimal ...
Koshal Shrestha , Binita Bhattarai , Laxmi Devi Manandhar , Salma KC Rai , Arniko Pandey , Shanti Gurung   +5 more
doaj   +1 more source

Probing for congenital nasolacrimal duct obstruction: a systematic review and meta-analysis of randomized clinical trials

, 2021
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], Jorge, Eliane Chaves [UNESP], Santos, Felipe Gasparini dos [UNESP], Farat, Joyce Godoy [UNESP], Fernandes Sousa Meneghim, Roberta Lilian [UNESP], Schellini, Silvana Artioli [UNESP]   +5 more
core   +1 more source

Refraction in Children with Unilateral and Bilateral Congenital Nasolacrimal Duct Obstruction [PDF]

Journal of Biomedical & Clinical Research, 2019
The study aimed to identify the type of refraction in children with unilateral and bilateral congenital nasolacrimal duct obstruction (CNLDO) who underwent nasolacrimal duct probing.
Krasina Valcheva, Snejana Murgova
doaj   +3 more sources

De Novo Complex Genomic Rearrangement Spanning 2q31.1 in a Proband With Congenital Malformations: Genotype–Phenotype Correlation and Development of a CGR Detection Pipeline

American Journal of Medical Genetics Part A, Volume 200, Issue 8, Page 1832-1841, August 2026.
ABSTRACT The 2q31 region is commonly associated with pathogenic alleles of the HOXD cluster leading to various clinical phenotypes related to skeletal development. We present a proband with tetralogy of Fallot and multiple congenital anomalies. Genomic variant screening including an in‐house CGR detection pipeline pairing genome sequencing (GS ...
Katherine Helle, Jesse D. Bengtsson, Mira Gandhi, Christopher M. Grochowski, Ming Yin Lun, Neha Sudhir, Shalini N. Jhangiani, Fritz J. Sedlazeck, Seema R. Lalani, Neil A. Hanchard, Claudia M. B. Carvalho   +10 more
wiley   +1 more source

Resolution of congenital nasolacrimal duct obstruction with conservative management

, 2017
Congenital nasolacrimal duct obstruction is the commonly encountered congenital anomaly in pediatric population occurring in as many as 30% of new borns. Conservative management of such condition with topical antibiotics and properly performed massage of
J B Shrestha
core   +1 more source

Common Ophthalmic Conditions in Popular Dog Breeds in Japan: Insights From a Survey of 105 Veterinarians Practicing Ophthalmology

Veterinary Ophthalmology, Volume 29, Issue 4, July 2026.
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, Arisu Kobayashi, Yasuyoshi Umeda, Susumu Hirashima, Yuichiro Muramatsu, Mitsuharu Ota, Makoto Yamashita, Yukako Kobayashi, Keiko Miyadera   +8 more
wiley   +1 more source

KDM2B‐Related Neurodevelopmental Disorder A Case‐Series Supporting the CxxC Domain Phenotype With Emphasis on Ocular and Dermatologic Features

American Journal of Medical Genetics Part A, Volume 200, Issue 5, Page 1098-1104, May 2026.
ABSTRACT The KDM2B‐related neurodevelopmental disorder is a recently identified Mendelian disorder of the epigenetic machinery associated with pathogenic variants in KDM2B. Global developmental delay, intellectual disability, congenital anomalies, and systemic manifestations characterize the disorder.
Adriana Gomes, Álvaro Martín‐Rodríguez, Miguel Del Campo, Lynne M. Bird   +3 more
wiley   +1 more source

Predictors of amblyogenic refractive errors in congenital nasolacrimal duct obstruction.

, 2019
Predictors of amblyogenic refractive errors in congenital nasolacrimal duct obstruction.
Namju Kim (760293), Sang-In Khwarg (6837074), Ho-Kyoung Choung (6837071), Hee Kyung Yang (655111), Jeong-Min Hwang (655113), YungJu Yoo (6837068)   +5 more
core   +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