Results 51 to 60 of about 36,048 (304)

Prevalence of Dental Anomalies in a Sample of Turkish Children: A Retrospective Study

open access: yesBezmiâlem Science
Objective: The aim of this study was to determine the prevalence of dental anomalies in Turkish children aged 2-14 years by panoramic radiographies. The most common dental anomaly, the frequency of multiple dental anomalies and gender differences were ...
Pınar SERDAR EYMİRLİ   +2 more
doaj   +1 more source

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

open access: yes, 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   +3 more
core   +1 more source

Gastrointestinal Manifestations in Rubinstein‐Taybi Syndrome

open access: yesAmerican 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   +3 more
wiley   +1 more source

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

open access: yesAmerican 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   +2 more
wiley   +1 more source

Dens invaginatus: A review and case series

open access: yesSaudi Endodontic Journal, 2018
Dens invaginatus (DI) (dens in dente) is a developmental anomaly resulting from an invagination in part of variable depth of the enamel organ into the dental papilla in the surface of the crown before calcification of the dental tissues.
Nesrine Tebbeb   +3 more
doaj   +1 more source

A case report of cornelia de lange syndrome in Northern Iran; a clinical and diagnostic study [PDF]

open access: yes, 2016
As a rare multisystem congenital anomaly disorder, Cornelia de Lange syndrome (CdLS) is featured by delayed growth and development, distinct facial dimorphism, limb malformations and multiple organ defects.
Alaee, E.   +2 more
core   +1 more source

Phenotype Expansion of Malan Syndrome: New Cases and a Review of the Literature

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Malan syndrome is an ultra‐rare overgrowth syndrome caused by pathogenic variants or deletions in nuclear factor one X (NFIX) located at 19p13.2. Here, we report a comprehensive literature review and phenotyping of known patients with Malan syndrome and present a novel cohort of eight patients.
Alex F. Nisbet   +10 more
wiley   +1 more source

Talon Cusp in A Supplementary Tooth - A Case Report

open access: yesJournal 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

open access: yesSelcuk 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   +5 more
doaj   +1 more source

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