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An unusual case of tricho–dento–osseous syndrome
Tricho–dento–osseous (TDO) syndrome is a multisystem congenital disorder that is known by bone, skin, and hair abnormalities. Primitive studies show different varieties of manifestations related to this disorder, which involve sclerotic bones, nail involvement, enamel hypoplasia, mandibular prognath...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8045528/ https://www.ncbi.nlm.nih.gov/pubmed/33889355 |
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author | Haghighat, Abbas Pourarz, Sobhan Ghazizadeh, Maryam Talebzadeh, Zahra |
author_facet | Haghighat, Abbas Pourarz, Sobhan Ghazizadeh, Maryam Talebzadeh, Zahra |
author_sort | Haghighat, Abbas |
collection | PubMed |
description | Tricho–dento–osseous (TDO) syndrome is a multisystem congenital disorder that is known by bone, skin, and hair abnormalities. Primitive studies show different varieties of manifestations related to this disorder, which involve sclerotic bones, nail involvement, enamel hypoplasia, mandibular prognathism, and taurodontism. Although exploring different TDO cases revealed genetic mutations in all of them, they have many variations in phenotypic view. In this study, we report a case whose primary diagnosis was alopecia and came for extraction of her third molars, but after clinical and radiographic examination, it was found that the cause of her disease was something different. |
format | Online Article Text |
id | pubmed-8045528 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-80455282021-04-21 An unusual case of tricho–dento–osseous syndrome Haghighat, Abbas Pourarz, Sobhan Ghazizadeh, Maryam Talebzadeh, Zahra Dent Res J (Isfahan) Case Report Tricho–dento–osseous (TDO) syndrome is a multisystem congenital disorder that is known by bone, skin, and hair abnormalities. Primitive studies show different varieties of manifestations related to this disorder, which involve sclerotic bones, nail involvement, enamel hypoplasia, mandibular prognathism, and taurodontism. Although exploring different TDO cases revealed genetic mutations in all of them, they have many variations in phenotypic view. In this study, we report a case whose primary diagnosis was alopecia and came for extraction of her third molars, but after clinical and radiographic examination, it was found that the cause of her disease was something different. Wolters Kluwer - Medknow 2020-12-10 /pmc/articles/PMC8045528/ /pubmed/33889355 Text en Copyright: © 2020 Dental Research Journal https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Haghighat, Abbas Pourarz, Sobhan Ghazizadeh, Maryam Talebzadeh, Zahra An unusual case of tricho–dento–osseous syndrome |
title | An unusual case of tricho–dento–osseous syndrome |
title_full | An unusual case of tricho–dento–osseous syndrome |
title_fullStr | An unusual case of tricho–dento–osseous syndrome |
title_full_unstemmed | An unusual case of tricho–dento–osseous syndrome |
title_short | An unusual case of tricho–dento–osseous syndrome |
title_sort | unusual case of tricho–dento–osseous syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8045528/ https://www.ncbi.nlm.nih.gov/pubmed/33889355 |
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