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Autosomal dominant mutation of MSX1 gene causing tooth and nail syndrome
Tooth and Nail Syndrome or Nail Dysplasias with Hypodontiaor Witkop´s Syndrome is an autosomal dominant condition present at birth and improves by age. An early diagnosis is essential to avoid future functional, aesthetic, and psychological problems. Here we report two classic cases with brief clini...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The African Field Epidemiology Network
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7908325/ https://www.ncbi.nlm.nih.gov/pubmed/33708320 http://dx.doi.org/10.11604/pamj.2020.36.229.23019 |
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author | Najmuddin, Mohammed Saheb, Safeena Abdul Khader Alharbi, Abdulrahman Nahi Alsobil, Fahad Mohammed Jhugroo, Chitra Khan, Aftab Ahmed Divakar, Darshan Devang Naik, Sachin Khanagar, Sanjeev Balappa |
author_facet | Najmuddin, Mohammed Saheb, Safeena Abdul Khader Alharbi, Abdulrahman Nahi Alsobil, Fahad Mohammed Jhugroo, Chitra Khan, Aftab Ahmed Divakar, Darshan Devang Naik, Sachin Khanagar, Sanjeev Balappa |
author_sort | Najmuddin, Mohammed |
collection | PubMed |
description | Tooth and Nail Syndrome or Nail Dysplasias with Hypodontiaor Witkop´s Syndrome is an autosomal dominant condition present at birth and improves by age. An early diagnosis is essential to avoid future functional, aesthetic, and psychological problems. Here we report two classic cases with brief clinical, radiological and genetic investigation along with a brief review of literature. |
format | Online Article Text |
id | pubmed-7908325 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The African Field Epidemiology Network |
record_format | MEDLINE/PubMed |
spelling | pubmed-79083252021-03-10 Autosomal dominant mutation of MSX1 gene causing tooth and nail syndrome Najmuddin, Mohammed Saheb, Safeena Abdul Khader Alharbi, Abdulrahman Nahi Alsobil, Fahad Mohammed Jhugroo, Chitra Khan, Aftab Ahmed Divakar, Darshan Devang Naik, Sachin Khanagar, Sanjeev Balappa Pan Afr Med J Case Report Tooth and Nail Syndrome or Nail Dysplasias with Hypodontiaor Witkop´s Syndrome is an autosomal dominant condition present at birth and improves by age. An early diagnosis is essential to avoid future functional, aesthetic, and psychological problems. Here we report two classic cases with brief clinical, radiological and genetic investigation along with a brief review of literature. The African Field Epidemiology Network 2020-07-29 /pmc/articles/PMC7908325/ /pubmed/33708320 http://dx.doi.org/10.11604/pamj.2020.36.229.23019 Text en Copyright: Mohammed Najmuddin et al. https://creativecommons.org/licenses/by/4.0 The Pan African Medical Journal (ISSN: 1937-8688). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Najmuddin, Mohammed Saheb, Safeena Abdul Khader Alharbi, Abdulrahman Nahi Alsobil, Fahad Mohammed Jhugroo, Chitra Khan, Aftab Ahmed Divakar, Darshan Devang Naik, Sachin Khanagar, Sanjeev Balappa Autosomal dominant mutation of MSX1 gene causing tooth and nail syndrome |
title | Autosomal dominant mutation of MSX1 gene causing tooth and nail syndrome |
title_full | Autosomal dominant mutation of MSX1 gene causing tooth and nail syndrome |
title_fullStr | Autosomal dominant mutation of MSX1 gene causing tooth and nail syndrome |
title_full_unstemmed | Autosomal dominant mutation of MSX1 gene causing tooth and nail syndrome |
title_short | Autosomal dominant mutation of MSX1 gene causing tooth and nail syndrome |
title_sort | autosomal dominant mutation of msx1 gene causing tooth and nail syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7908325/ https://www.ncbi.nlm.nih.gov/pubmed/33708320 http://dx.doi.org/10.11604/pamj.2020.36.229.23019 |
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