Results 31 to 40 of about 8,292 (221)

Congenital Nasolacrimal Duct Obstruction (CNLDO): A Review

Diseases, 2018
Congenital nasolacrimal duct obstruction (CNLDO) is a common condition causing excessive tearing or mucoid discharge from the eyes, due to blockage of the nasolacrimal duct system.
Aldo Vagge, Lorenzo Ferro Desideri, Paolo Nucci, Massimiliano Serafino, Giuseppe Giannaccare, Andrea Lembo, Carlo Enrico Traverso   +6 more
doaj   +1 more source

Adult nasolacrimal duct obstruction

Journal of Osteopathic Medicine, 1994
Abstract Tear production resulting from obstruction of the nasolacrimal duct is a common ophthalmic problem. The diagnosis and treatment of this condition require a thorough understanding of the lacrimal apparatus and its ocular and nasal relationships. Idiopathic or primary acquired nasolacrimal duct obstruction is a syndrome of unknown
C, Shermetaro, G J, Gladstone
openaire   +2 more sources

Morphometric evaluation of nasolacrimal duct

Anatomy, 2021
Objectives: Obstructions are very commonly seen in nasolacrimal duct before it opens into the inferior nasal meatus. Detailed anatomical knowledge of the nasolacrimal duct is crucial for physicians to understand the etiology of the obstructions, to plan ideal management option and to reduce unexpected iatrogenic injuries during surgeries.
Burcu Erçakmak Güneş, Alper Vatansever, Deniz Demiryürek, Ekim Gümeler   +3 more
openaire   +5 more sources

Nasal and Sinus Disorders in Patients with Primary Acquired Nasolacrimal Duct Obstruction (PANDO) [PDF]

Patient Safety and Quality Improvement Journal
Introduction:To investigate the frequency of nasal and sinus problems in patients with acquired nasolacrimal duct obstruction.Materials and Methods: The prospective case-control study was performed on 44 patients with primary acquired nasolacrimal duct ...
Mohammad Sharifi
doaj   +1 more source

Dependence of radioactive iodine-131 capture by the lacrimal ducts on the tear production level

Indian Journal of Ophthalmology, 2023
Purpose: Secondary acquired lacrimal duct obstruction (SALDO) is one of the complications of radioiodine therapy. SALDO is formed a few months after therapy if there is a sufficient uptake of radioactive iodine by the nasolacrimal duct.
Vasily D Yartsev, Marina S Sheremeta, Alexey A Trukhin, Eugenia L Atkova, Mikhail V Degtyarev, Valentina S Yasyuchenya, Danila V Yudakov   +6 more
doaj   +1 more source

OUTCOME OF INITIAL 100 CASES OF ENDOSCOPIC DACRYOCYSTORHINOSTOMY IN KIRKUK

Al-Kitab Journal for Pure Sciences, 2022
This study aimed at determining the effect and safety of endoscopic dacryocystorhinostomy (ENDO-DCR) in initial 100 cases of nasolacrimal duct obstruction. This study was done in Kirkuk general hospital from 2010 to 2017 with a total of 100 cases.
Tunjai namiq faiq
doaj   +1 more source

Rhinologist’s Endoscopic Experience of Lower Lacrimal System Pathologies in Paediatric Patients

Delhi Journal of Ophthalmology, 2017
Cases of congenital nasolacrimal duct block with unsuccessful blind probing were taken up for a repeat probing under endoscopic assistance. Membranes with a wide variation in thickness were found blocking the lower end of nasolacrimal duct.
Nishi Gupta
doaj   +1 more source

Lacrimal Plasty with Dacryocystorhinostomy-Anastomosis Using Microsurgery

Plastic and Reconstructive Surgery, Global Open, 2023
Background:. Dacryocystorhinostomy (DCR) is the standard treatment for nasolacrimal duct obstruction, but it has the disadvantage of creating a raw surface, which may lead to reocclusion due to the development of postoperative granulation tissue. In this
Daisuke Yanagisawa, MD, Shunsuke Yuzuriha, PhD   +1 more
doaj   +1 more source

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, EarlyView.
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

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, EarlyView.
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