نتایج جستجو برای: syndromic cleft

تعداد نتایج: 19425  

Journal: :Frontiers in Pediatrics 2021

To investigate whether the craniofacial sagittal jaw relationship in patients with non-syndromic cleft differed from non-cleft (NC) individuals by artificial intelligence (A.I.)-driven lateral cephalometric (Late. Ceph.) analysis. The study group comprised 123 subjects different types of clefts including 29 = BCLP (bilateral lip and palate), 41 UCLP (unilateral 9 UCLA alveolus), 13 UCL lip) NC ...

2017
Wasiu L Adeyemo Azeez Butali

Orofacial clefts (OFC) are complex birth defects. Studies using contemporary genomic techniques, bioinformatics, and statistical analyses have led to appreciable advances in identifying the causes of syndromic forms of clefts. This commentary gives an overview of the important cleft gene discoveries found using various genomic methods and tools.

Journal: :Cell cycle 2007
Tuula Rinne Hans G Brunner Hans van Bokhoven

Heterozygous mutations in the transcription factor gene p63 are causative for several syndromes, with ectodermal dysplasia, orofacial clefting and limb malformations as the key characteristics. Different combinations of these features are seen in five different syndromes, of which ectrodactyly, ectodermal dysplasia and cleft lip/palate syndrome (EEC) is the most common one. Mutations in p63 can...

Journal: :European journal of orthodontics 2015
Ahmet A Celebi Faruk I Ucar Ahmet E Sekerci Murat Caglaroglu Enes Tan

OBJECTIVE The aim of this study was to evaluate 1. the differences among the cleft sides of unilateral cleft lip and palate (UCLP) patients, non-cleft sides of the same UCLP patients and well matched control patients in the root development and position of permanent upper central incisors and 2. possible gender differences. MATERIALS AND METHODS The study sample consisted of 40 patient (20 ma...

Journal: :Archives of disease in childhood 2006
A Habel N Elhadi B Sommerlad J Powell

AIMS To identify prevalence of delayed detection of cleft palate, and associated factors that could lead to improved identification at neonatal clinical examination. METHODS Audit of hospital notes, parental questionnaire incorporating open ended questions, and telephone questionnaire of junior doctors in the referring hospitals incorporating fixed choice questions. RESULTS Of 344 cleft pal...

Journal: :iranian journal of basic medical sciences 0
asghar ebadifar dentofacial deformities research center, research institute of dental sciences, shahid beheshti university of medical sciences, tehran, iran roya hamedi dental carries prevention research center, qazvin university of medical sciences, qazvin, iran hamid reza khorramkhorshid genetic research centre, university of social welfare and rehabilitation sciences, tehran, iran koorosh kamali department of public health, school of public health, zanjan university of medical sciences, zanjan, iran fatemeh aghakhani moghadam bachelors of medical laboratory sciences, university of social welfare and rehabilitation sciences, tehran, iran

objective(s):we investigated the influence of genetic variation of the transforming growth-factor alpha (tgfa) locus on the relationship between smoking and oral clefts. materials and methods:in this study 105 iranian infants with non-syndromic cleft lip/palate and 218 controls with non-cleft birth defects were examined to test for associations among maternal exposures, genetic markers, and ora...

Journal: :The Journal of craniofacial surgery 2003
Dane St John Lori Pai Myron L Belfer John B Mulliken

The purpose of this study was to determine rates of divorce in parents of children with various types of craniofacial anomalies and to analyze possible confounding factors. A 29-question survey was sent to parents of all children evaluated in the Craniofacial Centre between 1992 and 1997. Parents were questioned regarding pre- and postnatal marital stability, whether the child's facial anomaly ...

Journal: :Gene 2016
Yirui Wang Yimin Sun Yongqing Huang Yongchu Pan Zhonglin Jia Lijuan Ma Lan Ma Feifei Lan Yuxi Zhou Jiayu Shi Xiong Yang Lei Zhang Hongbing Jiang Min Jiang Aihua Yin Jing Cheng Lin Wang Yinxue Yang Bing Shi

Cleft lip with or without cleft palate (CL/P) is one of the most common birth defects worldwide and is characterized by abnormalities of the orofacial structure. Syndromic CL/P is mainly caused by Mendelian disorders such as Van der Woude Syndrome (VWS). However, >70% of CL/P cases are nonsyndromic, characterized by isolated orofacial cleft without any known syndrome. The etiology of nonsyndrom...

2016
Hale Demir Tülin Kılıçaslan Öztürk Zerrin Calay Şennur İlvan Fuat Demirkıran

Sex cord-stromal tumors with annular tubules (SCTAT) of the ovary are rare. They have two clinical presentation forms: the syndromic form, which is associated with Peutz-Jeghers syndrome, and the non-syndromic form, which is frequently seen in the second or third decades. We describe a 13-year-old patient who underwent left oophorectomy. Macroscopically, the mass was 16×13×8 cm in diameter, enc...

2017
Renu Tanwar Vipul Jaitly Aadya Sharma Rashmi Heralgi Munish Ghangas Ankur Bhagat

Hyperdontia or supernumerary teeth in both arches without any syndromic manifestation are extremely rare. Supernumerary teeth are commonly associated with Gardner's syndrome, cleft lip and palate, cleidocranial dysplasia and trichorhinopha-langeal syndrome. Five cases of non-syndromic multiple premolars of maxillary and mandibular arches in Indian patients are presented here. This case series r...

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