Results 51 to 60 of about 1,678 (170)

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

On the Maxillofacial Development of Mice, Mus musculus

Journal of Morphology, Volume 286, Issue 3, March 2025.
This study focused on the craniofacial development of the mouse (Mus musculus), particularly the maxillofacial region. Using three‐dimensional reconstructions of histological sections combined with whole‐mount staining, we provided a detailed description of skeletal, neural, and vascular formation from the pharyngula (9.0 dpc) to late fetal stages (18 ...
Hiroki Higashiyama, Shunya Kuroda, Akiyasu Iwase, Naoki Irie, Hiroki Kurihara   +4 more
wiley   +1 more source

Adult nasolacrimal duct cyst presenting as an intranasal mass: Combined endoscopic marsupialization and dacryocystorhinostomy

Otolaryngology Case Reports
Nasolacrimal duct cysts are rare congenital anomalies that typically present in neonates and often resolve spontaneously. Persistence into adulthood is exceptionally uncommon and may pose diagnostic challenges when presenting as an intranasal mass.We ...
Mingda Yang, Lianhe Li, Yan Wang
doaj   +1 more source

Retrospective study in 1020 cases on the rate of surgical site infections after lacrimal surgery without prophylactic systemic antibiotics

Acta Ophthalmologica, Volume 102, Issue 8, Page 963-967, December 2024.
Abstract Background/Aims Data regarding the effectiveness of prophylactic systemic antibiotics (PSA) in lacrimal surgery is scarce. Therefore, we determined the postoperative surgical site infection (SSI) rate in lacrimal surgery without PSA. Methods We retrospectively analysed files of patients who underwent external (extDCR) or endoscopic endonasal ...
R. O. B. de Keizer, J. S. Suwandi, J. C. van Limpt, C. Kluis, G. Hötte, A. P. Nagtegaal, D. Paridaens   +6 more
wiley   +1 more source

Sella turcica and facial bones: Morphological integration in the human fetal cranium

Orthodontics &Craniofacial Research, Volume 27, Issue 6, Page 938-949, December 2024.
Abstract Objectives The cranial base plays a significant role in facial growth, and closer analyses of the morphological relationship between these two regions are needed to understand the morphogenesis of the face. Here, we aimed to study morphological integration between the sella turcica (ST) and facial bones during the fetal period using geometric ...
Natsuko Utsunomiya, Motoki Katsube, Yutaka Yamaguchi, Masanori Kumakiri, Naoki Morimoto, Shigehito Yamada   +5 more
wiley   +1 more source

Unilateral congenital dacryocele

PAMJ Clinical Medicine, 2020
We report a case of a healthy, full term, 3 months old boy, who was referred for evaluating a bluish-gray cystic mass, measuring approximately 1-cm just below the medial canthal tendon of the right eye, present since birth.
Narjisse Taouri
doaj   +1 more source

Childhood glaucoma: Implications for genetic counselling

Clinical Genetics, Volume 106, Issue 5, Page 545-563, November 2024.
Venn diagram representation of genes for which pathogenic variants have been identified to cause various types of childhood glaucoma. This diagram represents the genetic and phenotypic heterogeneity of childhood glaucoma illustrating the need for informed genetic counselling and testing as part of a multidisciplinary approach.
Giorgina Maxwell, Emmanuelle Souzeau
wiley   +1 more source

Endonasal endoscopic dacryocystorhinostomy in the paediatric population [PDF]

Rhinology Online, 2019
Background: Congenital nasolacrimal duct obstruction is frequent and paediatric endonasal endoscopic dacryocystorhinostomy (DCR) is increasingly used after conservative treatment failure.
Carla C. Moreira, Isabel M. Correia, Inês S. Cunha, Herédio Sousa, Ezequiel Barros   +4 more
doaj   +1 more source

Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)

American Journal of Medical Genetics Part A, Volume 194, Issue 10, October 2024.
Abstract Myhre syndrome is an increasingly diagnosed ultrarare condition caused by recurrent germline autosomal dominant de novo variants in SMAD4. Detailed multispecialty evaluations performed at the Massachusetts General Hospital (MGH) Myhre Syndrome Clinic (2016–2023) and by collaborating specialists have facilitated deep phenotyping, genotyping and
Angela E. Lin, Eleanor R. Scimone, Robyn P. Thom, Duraisamy Balaguru, T. Bernard Kinane, Peter P. Moschovis, Michael S. Cohen, Weizhen Tan, Cole D. Hague, Katelyn Dannheim, Lynne L. Levitsky, Evelyn Lilly, Daniel V. DiGiacomo, Kara M. Masse, Sarah M. Kadzielski, Claire A. Zar‐Kessler, Leo C. Ginns, Ann M. Neumeyer, Mary K. Colvin, Jack S. Elder, Christopher P. Learn, Hongmei Mou, Kathryn M. Weagle, Karen A. Buch, William E. Butler, Kenda Alhadid, Patricia L. Musolino, Sadia Sultana, Dhrubajyoti Bandyopadhyay, Otto Rapalino, Zachary S. Peacock, Elizabeth L. Chou, Gena Heidary, Aaron T. Dorfman, Shaine A. Morris, James D. Bergin, Jonathan H. Rayment, Lisa A. Schimmenti, Mark E. Lindsay, MGH Myhre Syndrome Study Group, Luisa Paredes Acosta, Jennifer A. Bassetti, Sarah Bowdin, Joy A. Bress, Joseph A. Camarda, Joanne S. Chiu, C. Eduardo Corrales, Gregory Costain, Mary Beth P. Dinulos, Rajiv Devanagondi, Emily S. Doherty, John Dykes, Ann‐Christine Duhaime, Robert F. English, Elizabeth Fieg, Nora D. B. Friedman, Carl P. Garabedian, Samantha Glowacki, Barbara R. Gottlieb, Mary Hope Griffin, Frances J. Hayes, Stephanie R. Hicks, Alicia M. Hinze, Brigette A. Jason, Joel Krier, Kristen Lindgren, Michael Lyons, Adnan Majid, Hannah C. Mannem, Marie McDonald, Vinod Misra, Amy Morgan, Barbara J. Nath, Michele Ploutz, Eloise J. Prijoles, Margaret B. Pulsifer, Alicia M. Quesnel, Farrah Rajabi, Mersedeh Rohanizadegan, Ana Maria Rosales, Holly Rothermel, Edith Schussler, Elizabeth A. Sellars, Joseph Shieh, Stephanie Sherrill, Heidi Taska‐Tench, Matthew Thompson, George E. Tiller, Stephanie E. Vallee, David Viskochil, Stephanie Ware, Rachel C. Whooten, Samuel Yang, Elaine H. Zackai, Dala Zakaria   +94 more
wiley   +1 more source

Clinical Characteristics, Genetic Analysis, and Literature Review of Cornelia de Lange Syndrome Type 4 Associated With a RAD21 Variant

Molecular Genetics &Genomic Medicine, Volume 12, Issue 9, September 2024.
Whole exome sequencing revealed a pathogenic variant c.1143G>A (p.Trp381*) in the RAD21 gene. We reviewed 36 patients with CdLS related to RAD21 gene variants reported worldwide. Frameshift variants constituted the predominant variant type, representing 36% (13/36) of cases.
Xinyu Yue, Meiping Chen, Xiaoan Ke, Hongbo Yang, Fengying Gong, Linjie Wang, Lian Duan, Hui Pan, Huijuan Zhu   +8 more
wiley   +1 more source