Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Palatal abnormalities"'
Autor:
Vera Lúcia Gil-da-Silva-Lopes, Agnes Cristina Fett-Conte, Fabíola Paoli Monteiro, Isabella Lopes Monlleó, Marshall Italo Barros Fontes, Ilária Cristina Sgardioli, Gabriela F. Leal, Erlane Marques Ribeiro, Têmis Maria Félix, Josiane Souza, Társis Paiva Vieira
Publikováno v:
The Cleft Palate-Craniofacial Journal. 52:411-416
Objectives The aim of this study was to describe clinical features in subjects with palatal abnormalities and to assess the distribution of these features among those with and without 22q11.2 deletion. Design Descriptive cohort. Patients One hundred
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7f2fa2dff7512dbdf77a2ea20e0945d
https://doi.org/10.1597/13-233
https://doi.org/10.1597/13-233
Publikováno v:
Çağdaş Tıp Dergisi, Vol 1, Iss 1, Pp 25-28 (2014)
Dil; konuşma, çiğneme , tatma ve yutma gibi birçok fonksiyona sahip, vücudumuzun en hareketli organıdır. Literatürde dilin sayısız konjenital ve kalıtımsal bozuklukları bildirilmiştir. Mikroglossi olarak da bilinen hipoglossi nadir anom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::59ec0d48cf851854adedbfd55f2c087e
http://dergipark.gov.tr/gopctd/issue/7309/95640?publisher=selcuk
http://dergipark.gov.tr/gopctd/issue/7309/95640?publisher=selcuk
Akademický článek
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Publikováno v:
Çağdaş Tıp Dergisi, Vol 1, Iss 1, Pp 25-28 (2011)
Volume: 1, Issue: 1 25-28
Çağdaş Tıp Dergisi
Volume: 1, Issue: 1 25-28
Çağdaş Tıp Dergisi
Tongue is the most mobile organ of the body with multiple functions such as speech, mastication, taste and swallowing. Numerous congenital and developmental disorders of the tongue have been reported in literature. Hypoglossia also known as microglos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::ff5c9400625a6c39acfc75b49714e462
http://www.scopemed.org/fulltextpdf.php?mno=11420
http://www.scopemed.org/fulltextpdf.php?mno=11420
Kniha
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Publikováno v:
International Journal of Phonosurgery & Laryngology. 2:85-87
Tongue is the most mobile organ of the body with multiple functions, such as speech, mastication, taste and swallowing. Numerous congenital and developmental disorders of the tongue have been reported in literature. Hypoglossia, also known as microgl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abddc41760d1b8395f5c27165b32f309
https://doi.org/10.5005/jp-journals-10023-1046
https://doi.org/10.5005/jp-journals-10023-1046
Publikováno v:
Clinics in plastic surgery. 41(2)
The 22q11.2 deletion syndrome (22q11DS) may be associated with several palatal abnormalities, including overt cleft palate, submucosal cleft palate, palatopharyngeal disproportion, and velar hypotonia. The syndrome is the genetic disorder most common
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afd7674ba4947b63a271ec493f9c0883
https://pubmed.ncbi.nlm.nih.gov/24607194
https://pubmed.ncbi.nlm.nih.gov/24607194
Autor:
Tom J. Ahern
Publikováno v:
Journal of Equine Science. 7:55-58
A number of palatal abnormalities had been previously reported and these were all diagnosed by utilising nasopharyngeal endoscopy. These included clefts, hypoplasia, cysts, cicatrices and iatrogenic defects of the soft palate. Three cases of defects
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0f99f4ebe347b70e478cb3649529f5d
https://doi.org/10.1294/jes.7.55
https://doi.org/10.1294/jes.7.55
Publikováno v:
Microscopy and Microanalysis. 15:5-6
The 22q11.2 microdeletion is found in most of DiGeorge and velocardiofacial syndromes. These individuals have a wide range of anomalies including congenital heart disease, palatal abnormalities, characteristic facial features, hypocalcaemia, immune d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a40394737343f3a8f683156c85ac100
https://doi.org/10.1017/s1431927609990481
https://doi.org/10.1017/s1431927609990481
Akademický článek
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