نتایج جستجو برای: philtrum

تعداد نتایج: 262  

Journal: :Pediatric dentistry 1985
S Wilson V Escobar J H Hersch B S Haskell

A report of a child with Cohen syndrome is presented. Of particular interest to dentists are the relatively consistent findings of open mouth, short philtrum, micrognathia, and the prominent maxillary central incisors. A combination of these findings in addition to other traits such as hypotonicity, variable degrees of mental retardation, narrow hands and feet, childhood obesity, and delayed pu...

2013
Kyung-Suk Cha

OBJECTIVE To standardize the facial soft-tissue characteristics of South Korean adults according to gender by measuring the soft-tissue thickness of young men and women with normal facial profiles by using three-dimensional (3D) reconstructed models. METHODS Computed tomographic images of 22 men aged 20 - 27 years and 18 women aged 20 - 26 years with normal facial profiles were obtained. The ...

2012
Robert J. Lipinski Peter Hammond Shonagh K. O’Leary-Moore Jacob J. Ament Stephen J. Pecevich Yi Jiang Francois Budin Scott E. Parnell Michael Suttie Elizabeth A. Godin Joshua L. Everson Deborah B. Dehart Ipek Oguz Hunter T. Holloway Martin A. Styner G. Allan Johnson Kathleen K. Sulik

Prenatal ethanol exposure is the leading preventable cause of congenital mental disability. Whereas a diagnosis of fetal alcohol syndrome (FAS) requires identification of a specific pattern of craniofacial dysmorphology, most individuals with behavioral and neurological sequelae of heavy prenatal ethanol exposure do not exhibit these defining facial characteristics. Here, a novel integration of...

Journal: :Birat Journal of Health Sciences 2022

A radicular cyst is an inflammatory odontogenic of the jaw commonly found at apices tooth anterior maxilla. It develops as a sequel untreated dental caries with pulp necrosis and periapical infection. Different treatment includes surgical endodontic treatment, extraction involving tooth, marsupialization, enucleation primary closure followed by rehabilitation. We presented case huge midline 52 ...

Journal: :IEEE Sensors Journal 2021

Recently, wearable electronics for health monitoring have been demonstrated with considerable benefits early-stage disease detection. This article reports a flexible, bending-insensitive, bio-compatible and lightweight respiration sensor. The sensor consists of highly oriented carbon nanotube (HO-CNT) films embedded between electro-spun polyacrylonitrile (PAN) layers. By aligning nanotubes the ...

2014
J. Cohen-Lévy

A young patient, 10 years of age (Fig. 1), was referred to us by her dentist for the correction of an excessive overjet, caused by finger sucking. She presented with delayed growth and short stature and was being treated for these conditions at a hospital facility. Initially it was difficult to examine her because she was very apprehensive. The extraoral examination revealed mildly atypical fac...

Journal: :Journal of medical genetics 1997
A Mégarbané N Souraty M Prieur D Theophile P Chédid J Augé M Vekemans

An 18 month old girl was referred to us because of dysmorphic features and psychomotor and growth retardation. On physical examination, she was found to have microcephaly, open fontanelles, a prominent forehead, a flat occiput, hypertelorism, sparse eyebrows, a small nose with a depressed nasal bridge, a bulging philtrum, a thin upper lip, a high arched palate, low set and posteriorly rotated e...

Journal: :Indian pediatrics 1995
B Kar

The propositus was a 12-month-old male born to non consanguineous parents at 3rd full term breech delivery. His weight was 7.4 kg, height was 65.5 cm and head circumference was 39 cm. The clinical examinations showed the features of deletion 9p syndrome, viz., trigonocephaly, flat nasal bridge, anteverted nares, long philtrum, wide spaced nipples, micrognathia, short stubby hands and the featur...

Journal: :Clinical genetics 2013
A Dixit S McKee S Mansour S G Mehta G A Tanteles V Anastasiadou P C Patsalis K Martin S McCullough M Suri A Sarkar

Williams-Beuren syndrome is a well-known microdeletion syndrome with a recognizable clinical phenotype. The subtle phenotype of the reciprocal microduplication of the Williams-Beuren critical region has been described recently. We report seven further patients, and a transmitting parent, with 7q11.23 microduplication. All our patients had speech delay, autistic features and facial dysmorphism c...

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