Results 51 to 60 of about 35,818 (311)

Multidisciplinary Approach to Fused Maxillary central Incisors: a Case Report [PDF]

, 2014
Introduction: The fusion of permanent teeth is a development anomaly of dental hard tissue. It may require a hard multidisciplinary approach with orthodontics, endodontics, surgery and prosthetics to solve aesthetic and functional problems.
Cerone V, Gasparro R, Riccitiello F, Sammartino G, Trosino O.   +4 more
core   +1 more source

Swallowing and Communication in Cockayne Syndrome: Clinical Characteristics and Management

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Cockayne syndrome (CS) is an ultrarare genetic disorder associated with genes encoding proteins involved in DNA repair. The clinical course of CS involves neurodevelopmental and neurodegenerative features, including swallowing and communication impairments.
Abigail M. Spoden, Katlyn E. McGrattan, Peter B. Kang   +2 more
wiley   +1 more source

Talon Cusp in A Supplementary Tooth - A Case Report

Journal of Indian Academy of Oral Medicine and Radiology, 2005
Talon cusp is a morphological dental anomaly, which presents as an accessory cusp and commonly occurs on the lingual surfaces of the incisors. Supernumerary tooth is a common dental anomaly, which occurs in both maxilla and the mandible.
S Meera, Babu Mathew
doaj  

Güneydoğu Anadolu Bölgesi’nde dental anomalilerin görülme sıklığı

Selcuk Dental Journal, 2018
Amaç: Bu çalışmanın amacı, Güneydoğu Anadolu Bölgesinde yaşayan bireylerde dental anomalilerin görülme sıklığının ve cinsiyetler arasındaki dental anomali görülme yatkınlıkların değerlendirilmesidir.Gereç ve Yöntemler: Çalışma Adıyaman Üniversitesi ...
Mahmut Koparal, Haluk Yener Ünsal, Hilal Türker Alan, Mustafa Yalçın, Bilal Ege, Belgin Gülsün   +5 more
doaj   +1 more source

Orthognathic Surgical Outcomes in Patients With and Without Craniofacial Anomalies [PDF]

, 2018
Purpose The objective of this study is to examine hospitalization outcomes after orthognathic surgery. This study tests the hypothesis that patients with craniofacial anomalies have higher billed hospital charges, longer lengths of stay, and increased ...
Allareddy, Veerasathpurush, Fletcher, Steven, Metalwala, Zohra, Okunseri, Christopher   +3 more
core   +1 more source

Gastrointestinal Manifestations in Rubinstein‐Taybi Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Rubinstein–Taybi syndrome is a rare genetic condition associated with a wide range of physical, cognitive, and developmental impairments, yet its gastrointestinal manifestations remain poorly characterized. Case reports and small series suggest a high prevalence of gastroesophageal reflux, constipation, dysphagia, and nutritional compromise ...
Mohamad Abi Nassif, Ajay Kaul, Lev Dorfman, Khalil El‐Chammas   +3 more
wiley   +1 more source

Prevalence of dental anomalies in Indian population [PDF]

, 2013
Objectives: Developmental anomalies of the dentition are not infrequently observed by the dental practitioner. The aim of the present study was to determine the prevalence of dental anomalies in the Indian population.
Bharati, Doni, Farzan, Rahman, Santosh, Patil, Sumita, Kaswan   +3 more
core  

Anomalous Chiral Fermi Surface

, 2012
We provide a geometrical argument for the emergence of a Wess-Zumino-Witten (WZW) term for a Fermi surface threaded by a Berry curvature. In the presence of external fields, the gauged WZW term yields a chiral (triangle) anomaly for the fermionic current
A. S. Gorsky, G. E. Volovik, Ismail Zahed, M. A. Nowak   +3 more
core   +1 more source

Dental Anomalies Associated with Craniometaphyseal Dysplasia [PDF]

Journal of Dental Research, 2014
Craniometaphyseal dysplasia (CMD) is a rare genetic disorder encompassing hyperostosis of craniofacial bones and metaphyseal widening of tubular bones. Dental abnormalities are features of CMD that have been little discussed in the literature. We performed dentofacial examination of patients with CMD and evaluated consequences of orthodontic movement ...
I-P, Chen, A, Tadinada, E H, Dutra, A, Utreja, F, Uribe, E J, Reichenberger   +5 more
openaire   +2 more sources

Expanding the Phenotype of TUFM‐Related Combined Oxidative Phosphorylation Deficiency 4

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Combined oxidative phosphorylation deficiency 4 (COXPD4) is a rare mitochondrial condition caused by biallelic deleterious variants in the nuclear‐encoded gene TUFM. To date, most individuals with COXPD4 have presented with encephalopathy, hypotonia, and abnormal brain imaging. Many of the reported individuals died in infancy. We aim to expand
Noémie Villeneuve‐Cloutier, Jodi Warman‐Chardon, Danielle K. Bourque   +2 more
wiley   +1 more source