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A Highlighted Case for Emphasizing on Clinical Diagnosis for Rare Syndrome in Third World
Premature tooth loss is a disastrous situation that affects deciduous or permanent teeth era with different causes. It may be attributed to some disorders like Papillon-Lefevre syndrome or coffin-lowry syndrome but because of ambiguous nature, precise diagnosis is not easily possible. Moreover, it h...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shahid Beheshti University of Medical Sciences
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703633/ https://www.ncbi.nlm.nih.gov/pubmed/29201128 |
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author | OWLIA, Fatemeh AKHAVAN KARBASSI, Mohammad-Hassan HAKIMIAN, Roqayeh ALEMRAJABI, Mohammad Sadegh |
author_facet | OWLIA, Fatemeh AKHAVAN KARBASSI, Mohammad-Hassan HAKIMIAN, Roqayeh ALEMRAJABI, Mohammad Sadegh |
author_sort | OWLIA, Fatemeh |
collection | PubMed |
description | Premature tooth loss is a disastrous situation that affects deciduous or permanent teeth era with different causes. It may be attributed to some disorders like Papillon-Lefevre syndrome or coffin-lowry syndrome but because of ambiguous nature, precise diagnosis is not easily possible. Moreover, it has very low incidence and defines by few and limited case series, with vague characters to some extent, confusion in detecting the right diagnosis is a common possibility. Hence, it is expectable to have a wrong diagnosis for this case. In this study, a 5-yr-old boy with chief complaint of early tooth loss despite having blindness in left eye and palmar keratosis is reported, although he had some other manifestation of oculodentodigital dysplasia (ODDD) like ataxia, dysarthria and nail deformity, ignoring other extra and intra oral finding. He was diagnosed as Papillon-Lefevre syndrome already, just because of early tooth loss and palmar keratosis. |
format | Online Article Text |
id | pubmed-5703633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Shahid Beheshti University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-57036332018-01-01 A Highlighted Case for Emphasizing on Clinical Diagnosis for Rare Syndrome in Third World OWLIA, Fatemeh AKHAVAN KARBASSI, Mohammad-Hassan HAKIMIAN, Roqayeh ALEMRAJABI, Mohammad Sadegh Iran J Child Neurol Case Report Premature tooth loss is a disastrous situation that affects deciduous or permanent teeth era with different causes. It may be attributed to some disorders like Papillon-Lefevre syndrome or coffin-lowry syndrome but because of ambiguous nature, precise diagnosis is not easily possible. Moreover, it has very low incidence and defines by few and limited case series, with vague characters to some extent, confusion in detecting the right diagnosis is a common possibility. Hence, it is expectable to have a wrong diagnosis for this case. In this study, a 5-yr-old boy with chief complaint of early tooth loss despite having blindness in left eye and palmar keratosis is reported, although he had some other manifestation of oculodentodigital dysplasia (ODDD) like ataxia, dysarthria and nail deformity, ignoring other extra and intra oral finding. He was diagnosed as Papillon-Lefevre syndrome already, just because of early tooth loss and palmar keratosis. Shahid Beheshti University of Medical Sciences 2017 /pmc/articles/PMC5703633/ /pubmed/29201128 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report OWLIA, Fatemeh AKHAVAN KARBASSI, Mohammad-Hassan HAKIMIAN, Roqayeh ALEMRAJABI, Mohammad Sadegh A Highlighted Case for Emphasizing on Clinical Diagnosis for Rare Syndrome in Third World |
title | A Highlighted Case for Emphasizing on Clinical Diagnosis for Rare Syndrome in Third World |
title_full | A Highlighted Case for Emphasizing on Clinical Diagnosis for Rare Syndrome in Third World |
title_fullStr | A Highlighted Case for Emphasizing on Clinical Diagnosis for Rare Syndrome in Third World |
title_full_unstemmed | A Highlighted Case for Emphasizing on Clinical Diagnosis for Rare Syndrome in Third World |
title_short | A Highlighted Case for Emphasizing on Clinical Diagnosis for Rare Syndrome in Third World |
title_sort | highlighted case for emphasizing on clinical diagnosis for rare syndrome in third world |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703633/ https://www.ncbi.nlm.nih.gov/pubmed/29201128 |
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