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Apert Syndrome: A Case Report
Apert syndrome (acrocephalosyndactyly) is a rare congenital disorder characterized by craniosynostosis, midfacial malformation and symmetrical syndactyly. We present a 10-month-old infant having all the features of classical Apert syndrome. How to cite this article: Khan S, Chatra L, Shenai P, Veena...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Jaypee Brothers Medical Publishers
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4155880/ https://www.ncbi.nlm.nih.gov/pubmed/25206168 http://dx.doi.org/10.5005/jp-journals-10005-1166 |
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author | Khan, Saba Chatra, Laxmikanth Shenai, Prashanth Veena, KM |
author_facet | Khan, Saba Chatra, Laxmikanth Shenai, Prashanth Veena, KM |
author_sort | Khan, Saba |
collection | PubMed |
description | Apert syndrome (acrocephalosyndactyly) is a rare congenital disorder characterized by craniosynostosis, midfacial malformation and symmetrical syndactyly. We present a 10-month-old infant having all the features of classical Apert syndrome. How to cite this article: Khan S, Chatra L, Shenai P, Veena KM. Apert Syndrome: A Case Report. Int J Clin Pediatr Dent 2012; 5(3):203-206. |
format | Online Article Text |
id | pubmed-4155880 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Jaypee Brothers Medical Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-41558802014-09-09 Apert Syndrome: A Case Report Khan, Saba Chatra, Laxmikanth Shenai, Prashanth Veena, KM Int J Clin Pediatr Dent Case Report Apert syndrome (acrocephalosyndactyly) is a rare congenital disorder characterized by craniosynostosis, midfacial malformation and symmetrical syndactyly. We present a 10-month-old infant having all the features of classical Apert syndrome. How to cite this article: Khan S, Chatra L, Shenai P, Veena KM. Apert Syndrome: A Case Report. Int J Clin Pediatr Dent 2012; 5(3):203-206. Jaypee Brothers Medical Publishers 2012 2012-12-05 /pmc/articles/PMC4155880/ /pubmed/25206168 http://dx.doi.org/10.5005/jp-journals-10005-1166 Text en Copyright © 2012; Jaypee Brothers Medical Publishers (P) Ltd. This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Case Report Khan, Saba Chatra, Laxmikanth Shenai, Prashanth Veena, KM Apert Syndrome: A Case Report |
title | Apert Syndrome: A Case Report |
title_full | Apert Syndrome: A Case Report |
title_fullStr | Apert Syndrome: A Case Report |
title_full_unstemmed | Apert Syndrome: A Case Report |
title_short | Apert Syndrome: A Case Report |
title_sort | apert syndrome: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4155880/ https://www.ncbi.nlm.nih.gov/pubmed/25206168 http://dx.doi.org/10.5005/jp-journals-10005-1166 |
work_keys_str_mv | AT khansaba apertsyndromeacasereport AT chatralaxmikanth apertsyndromeacasereport AT shenaiprashanth apertsyndromeacasereport AT veenakm apertsyndromeacasereport |