Palatoplasty in a patient with Seckel syndrome

We report a rare case of a patient of Seckel syndrome having cleft palate born to nonconsanguineous married parents. This 8-year-old male child underwent successful palatoplasty under general anesthesia. Till date there are approximately 60 cases of Seckel syndrome reported in the literature. The sy...

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Autores principales: Garg, Ramneesh, Uppal, Sanjeev, Mittal, Rajinder, Grewal, Anju, Sood, Dinesh, Shah, Sheerin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Case Report - Orofacial Clefts
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3591075/
https://www.ncbi.nlm.nih.gov/pubmed/23482443
http://dx.doi.org/10.4103/2231-0746.95324
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author Garg, Ramneesh
Uppal, Sanjeev
Mittal, Rajinder
Grewal, Anju
Sood, Dinesh
Shah, Sheerin
author_facet Garg, Ramneesh
Uppal, Sanjeev
Mittal, Rajinder
Grewal, Anju
Sood, Dinesh
Shah, Sheerin
author_sort Garg, Ramneesh
collection PubMed
description We report a rare case of a patient of Seckel syndrome having cleft palate born to nonconsanguineous married parents. This 8-year-old male child underwent successful palatoplasty under general anesthesia. Till date there are approximately 60 cases of Seckel syndrome reported in the literature. The syndrome which has autosomal recessive inheritance is characterized by Intra Uterine Growth Retardation, microcephaly, dwarfism, and bird-like face. The associated features of the syndrome and technical details of surgery and anesthesia are discussed.
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spelling pubmed-35910752013-03-11 Palatoplasty in a patient with Seckel syndrome Garg, Ramneesh Uppal, Sanjeev Mittal, Rajinder Grewal, Anju Sood, Dinesh Shah, Sheerin Ann Maxillofac Surg Case Report - Orofacial Clefts We report a rare case of a patient of Seckel syndrome having cleft palate born to nonconsanguineous married parents. This 8-year-old male child underwent successful palatoplasty under general anesthesia. Till date there are approximately 60 cases of Seckel syndrome reported in the literature. The syndrome which has autosomal recessive inheritance is characterized by Intra Uterine Growth Retardation, microcephaly, dwarfism, and bird-like face. The associated features of the syndrome and technical details of surgery and anesthesia are discussed. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3591075/ /pubmed/23482443 http://dx.doi.org/10.4103/2231-0746.95324 Text en Copyright: © Annals of Maxillofacial Surgery http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report - Orofacial Clefts
Garg, Ramneesh
Uppal, Sanjeev
Mittal, Rajinder
Grewal, Anju
Sood, Dinesh
Shah, Sheerin
Palatoplasty in a patient with Seckel syndrome
title Palatoplasty in a patient with Seckel syndrome
title_full Palatoplasty in a patient with Seckel syndrome
title_fullStr Palatoplasty in a patient with Seckel syndrome
title_full_unstemmed Palatoplasty in a patient with Seckel syndrome
title_short Palatoplasty in a patient with Seckel syndrome
title_sort palatoplasty in a patient with seckel syndrome
topic Case Report - Orofacial Clefts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3591075/
https://www.ncbi.nlm.nih.gov/pubmed/23482443
http://dx.doi.org/10.4103/2231-0746.95324
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