Goldenhar syndrome with new oral findings!

Goldenhar syndrome (GS) is a condition with a multitude of abnormalities, classically involving ocular and ear defects, hemifacial microsomia, and vertebral anomalies, which may also be associated with cardiovascular and renal malformations. It is a rare congenital anomaly of unclear etiology. The p...

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Autor principal: Vela D Desai
Formato: article
Lenguaje:EN
Publicado: Wolters Kluwer Medknow Publications 2021
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Acceso en línea:https://doaj.org/article/3db3425b016e402dae61131143cdd7b4
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spelling oai:doaj.org-article:3db3425b016e402dae61131143cdd7b42021-11-12T10:09:47ZGoldenhar syndrome with new oral findings!2348-33342348-506X10.4103/cjhr.cjhr_105_19https://doaj.org/article/3db3425b016e402dae61131143cdd7b42021-01-01T00:00:00Zhttp://www.cjhr.org/article.asp?issn=2348-3334;year=2021;volume=8;issue=2;spage=131;epage=133;aulast=Desaihttps://doaj.org/toc/2348-3334https://doaj.org/toc/2348-506XGoldenhar syndrome (GS) is a condition with a multitude of abnormalities, classically involving ocular and ear defects, hemifacial microsomia, and vertebral anomalies, which may also be associated with cardiovascular and renal malformations. It is a rare congenital anomaly of unclear etiology. The purpose of reporting this case of a 16-year-old boy with GS is, to update, the existing literature of new oral findings observed.Vela D DesaiWolters Kluwer Medknow Publicationsarticle medical evaluationmultidisciplinary approachsupernumerary teethsyndrome MedicineRNursingRT1-120ENCHRISMED Journal of Health and Research, Vol 8, Iss 2, Pp 131-133 (2021)
institution DOAJ
collection DOAJ
language EN
topic medical evaluation
multidisciplinary approach
supernumerary teeth
syndrome
Medicine
R
Nursing
RT1-120
spellingShingle medical evaluation
multidisciplinary approach
supernumerary teeth
syndrome
Medicine
R
Nursing
RT1-120
Vela D Desai
Goldenhar syndrome with new oral findings!
description Goldenhar syndrome (GS) is a condition with a multitude of abnormalities, classically involving ocular and ear defects, hemifacial microsomia, and vertebral anomalies, which may also be associated with cardiovascular and renal malformations. It is a rare congenital anomaly of unclear etiology. The purpose of reporting this case of a 16-year-old boy with GS is, to update, the existing literature of new oral findings observed.
format article
author Vela D Desai
author_facet Vela D Desai
author_sort Vela D Desai
title Goldenhar syndrome with new oral findings!
title_short Goldenhar syndrome with new oral findings!
title_full Goldenhar syndrome with new oral findings!
title_fullStr Goldenhar syndrome with new oral findings!
title_full_unstemmed Goldenhar syndrome with new oral findings!
title_sort goldenhar syndrome with new oral findings!
publisher Wolters Kluwer Medknow Publications
publishDate 2021
url https://doaj.org/article/3db3425b016e402dae61131143cdd7b4
work_keys_str_mv AT veladdesai goldenharsyndromewithneworalfindings
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