Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Malformed ears"'
Autor:
Cigdem Yuce Kahraman, Pelin Ercoskun
Publikováno v:
American Journal of Medical Genetics Part A. 185:617-619
Witteveen-Kolk syndrome is a rare genetic disorder characterized by intellectual disability, developmental delay and dysmorphic facial features including a long face with prominent forehead, depressed nasal bridge, long-smooth philtrum and malformed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2abdcd9fda50315e872bb96f7ccfb83f
https://doi.org/10.1002/ajmg.a.61950
https://doi.org/10.1002/ajmg.a.61950
Publikováno v:
The Journal of prosthetic dentistry. 128(5)
The surgical reconstruction of congenitally missing or malformed ears is challenging and involves complicated surgeries. Ear shape, position, and skin color will likely be compromised in patients with relative anatomic symmetry, and it is easier to r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::821cf6b732b2f82784d93a8d1018b61c
https://pubmed.ncbi.nlm.nih.gov/33795159
https://pubmed.ncbi.nlm.nih.gov/33795159
Autor:
Davide Soloperto, Daniele Marchioni, Livio Presutti, Luca Bianconi, Andrea Sacchetto, Luca Sacchetto, Marco Carner
Objective: Complex middle and inner ear malformations are considered an important limitation for cochlear implant (CI) with traditional microscopic techniques. The aim of the present study is to describe the results of the endoscopic-assisted CI proc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cffe72b85646d481f8253420511d15df
http://hdl.handle.net/11562/1036037
http://hdl.handle.net/11562/1036037
Autor:
María Luisa Fajardo-Loo, Leonor Contreras-Aguilar, Ismenia Gamboa-Oré, Dina Torres-Gonzáles, Jackeline Zevallos-Murgado, Ruth Barrientos-Marca, Sergio Talavera-Vargas-Machuca
Publikováno v:
Revista Peruana de Investigación Materno Perinatal, Vol 5, Iss 2 (2016)
Las deleciones cromosómicas son anomalías estructurales que originan pérdidas del material genómico ydependiendo de su extensión suelen dar lugar a condiciones genéticas irreversibles muy discapacitantes. Ladeleción intersticial del brazo cort
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa35463fe2068ae42ad7e4f22f903ca6
https://doi.org/10.33421/inmp.201670
https://doi.org/10.33421/inmp.201670
Akademický článek
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Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 15, Iss 2, Pp 199-202 (2014)
Background : Miller syndrome is one of the acrofacial dysostosis syndromes, which are characterized by malformations of the craniofacial region and limbs. Case report : A 26 month old male child, the product of healthy nonconsanguineous parents has m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a06ede9dac5835f1367c6a8635b22f7e
http://www.sciencedirect.com/science/article/pii/S1110863013000979
http://www.sciencedirect.com/science/article/pii/S1110863013000979
Publikováno v:
Journal of Radiology Case Reports. 10
We present a case of a 13-year-old boy with clinical features of Goldenhar syndrome (hemifacial microsomia with malformed ears) and associated contralateral pulmonary aplasia. The patient did not have any associated respiratory symptoms. Pulmonary ap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4e75538c834d2470d3c780f93bd3eaf
https://doi.org/10.3941/jrcr.v10i1.2113
https://doi.org/10.3941/jrcr.v10i1.2113
Autor:
Nayaret Soto, Patricio Encalada
Publikováno v:
Journal Of Oral Research. 1:81-85
En la literatura actual se puede encontrar amplia variedad de sindromes asociados a fisuras palatinas, por eso frente pacientes que presentan esta alteracion es fundamental preguntar si la afectacion esta o no asociada a algun tipo de sindrome polima
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f26c8deb19e5da544ca419942ef3d19
https://doi.org/10.17126/joralres.2012.017
https://doi.org/10.17126/joralres.2012.017
Autor:
N. Tsuji, H. Kawashima
Publikováno v:
Clinical Genetics. 31:303-307
We report a mother and son who have a microcephaly with a characteristic dysmorphic face. Prominent manifestations include facial asymmetry, prominent glabella, deafness, low-set, cup-shaped ears, thick, protruding lower lip, micrognathia, and mental
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17bf6a724236db18c13bdacd5f410576
https://doi.org/10.1111/j.1399-0004.1987.tb02812.x
https://doi.org/10.1111/j.1399-0004.1987.tb02812.x
Publikováno v:
Otologyneurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology. 36(3)
OBJECTIVE To report the use of the retrofacial approach for cochlear implantation in three cases of malformed ears with inaccessible round windows through the standard facial recess. PATIENTS Two children with bilateral profound sensorineural hearing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99194eda81ad9e146dfb48115788070d
https://pubmed.ncbi.nlm.nih.gov/25594386
https://pubmed.ncbi.nlm.nih.gov/25594386