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Multiple Hereditary Osteochondromatosis: A Case Report
OBJECTIVES: Common carious lesions owing to vomiting are not widespread in children. In this case, we aimed to report an 11-years-old male patient with common carious lesions due to repeated vomitings, chewing and eating difficulty and retarded growth with Multiple Hereditary Osteochondromatosis (MH...
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Formato: | Texto |
Lenguaje: | English |
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Dental Investigations Society
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2638239/ https://www.ncbi.nlm.nih.gov/pubmed/19212564 |
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author | Küçükesmen, Çiḡdem Özen, Buḡra Akçam, Mustafa |
author_facet | Küçükesmen, Çiḡdem Özen, Buḡra Akçam, Mustafa |
author_sort | Küçükesmen, Çiḡdem |
collection | PubMed |
description | OBJECTIVES: Common carious lesions owing to vomiting are not widespread in children. In this case, we aimed to report an 11-years-old male patient with common carious lesions due to repeated vomitings, chewing and eating difficulty and retarded growth with Multiple Hereditary Osteochondromatosis (MHO). CASE REPORT: An 11-years-old boy was referred to Department of Pediatric Dentistry in Faculty of Dentistry because of eating difficulty owing to common carious lesions. It was seen that the patient growth was generally retarded in extra-oral examination. Some exostoses were also present on the extremities. It was learned that he was previously diagnosed as MHO in Faculty of Medicine. Nausea and vomiting have been commonly occurring after taking of Didronat. Chewing and eating difficulty and inadequate nutrition were present because of bad oral hygiene, carious lesions and remained roots. Growth was negatively affected by malnutrition and MHO. RESULTS: Diet recommendations were given and oral hygiene behaviors were rearranged. Preventive, surgical, restorative and prosthetical dental applications were applied for dental treatments. |
format | Text |
id | pubmed-2638239 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Dental Investigations Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-26382392009-02-11 Multiple Hereditary Osteochondromatosis: A Case Report Küçükesmen, Çiḡdem Özen, Buḡra Akçam, Mustafa Eur J Dent Case Reports OBJECTIVES: Common carious lesions owing to vomiting are not widespread in children. In this case, we aimed to report an 11-years-old male patient with common carious lesions due to repeated vomitings, chewing and eating difficulty and retarded growth with Multiple Hereditary Osteochondromatosis (MHO). CASE REPORT: An 11-years-old boy was referred to Department of Pediatric Dentistry in Faculty of Dentistry because of eating difficulty owing to common carious lesions. It was seen that the patient growth was generally retarded in extra-oral examination. Some exostoses were also present on the extremities. It was learned that he was previously diagnosed as MHO in Faculty of Medicine. Nausea and vomiting have been commonly occurring after taking of Didronat. Chewing and eating difficulty and inadequate nutrition were present because of bad oral hygiene, carious lesions and remained roots. Growth was negatively affected by malnutrition and MHO. RESULTS: Diet recommendations were given and oral hygiene behaviors were rearranged. Preventive, surgical, restorative and prosthetical dental applications were applied for dental treatments. Dental Investigations Society 2007-07 /pmc/articles/PMC2638239/ /pubmed/19212564 Text en Copyright 2007 European Journal of Dentistry. All rights reserved. |
spellingShingle | Case Reports Küçükesmen, Çiḡdem Özen, Buḡra Akçam, Mustafa Multiple Hereditary Osteochondromatosis: A Case Report |
title | Multiple Hereditary Osteochondromatosis: A Case Report |
title_full | Multiple Hereditary Osteochondromatosis: A Case Report |
title_fullStr | Multiple Hereditary Osteochondromatosis: A Case Report |
title_full_unstemmed | Multiple Hereditary Osteochondromatosis: A Case Report |
title_short | Multiple Hereditary Osteochondromatosis: A Case Report |
title_sort | multiple hereditary osteochondromatosis: a case report |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2638239/ https://www.ncbi.nlm.nih.gov/pubmed/19212564 |
work_keys_str_mv | AT kucukesmencigdem multiplehereditaryosteochondromatosisacasereport AT ozenbugra multiplehereditaryosteochondromatosisacasereport AT akcammustafa multiplehereditaryosteochondromatosisacasereport |