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- Publisher Website: 10.1186/s12903-016-0266-0
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- PMID: 27531358
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Article: Current concepts in odontohypophosphatasia form of hypophosphatasia and report of two cases
Title | Current concepts in odontohypophosphatasia form of hypophosphatasia and report of two cases |
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Authors | |
Keywords | Alkaline phosphatase Cone-beam computed tomography Dysplasia Hyperthyroidism Radicular cyst Short root anomaly |
Issue Date | 2016 |
Publisher | BioMed Central Ltd. The Journal's web site is located at http://www.biomedcentral.com/bmcoralhealth/ |
Citation | BMC Oral Health, 2016, v. 16, article no. 70 How to Cite? |
Abstract | Background:
Hypophosphatasia is a rare inherited disease derived from mutations in tissue non-specific alkaline phosphatase genes, with typical oral symptoms including short root anomaly and dysplasia of dentin or cementum.
Case presentation:
Two young female patients presented with short root anomaly with a history of premature loss of deciduous and/or permanent teeth. The laboratory and imaging investigations were performed. One case was diagnosed as odontohypophosphatasia concurrent with hyperthyroidism, the other was odontohypophosphatasia concurrent with multiple radicular cysts.
Conclusion:
This report presents two cases of odontohypophosphatasia, a rare disease which is difficult to be diagnosed, and highlights that the history of premature loss of deciduous and/or permanent teeth, oral manifestation and laboratory tests are crucial for clinical diagnosis. |
Persistent Identifier | http://hdl.handle.net/10722/238630 |
ISSN | 2023 Impact Factor: 2.6 2023 SCImago Journal Rankings: 0.737 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Wang, ZY | - |
dc.contributor.author | Zhang, K | - |
dc.contributor.author | Zheng, GS | - |
dc.contributor.author | Qiao, W | - |
dc.contributor.author | Su, Y | - |
dc.date.accessioned | 2017-02-20T01:24:00Z | - |
dc.date.available | 2017-02-20T01:24:00Z | - |
dc.date.issued | 2016 | - |
dc.identifier.citation | BMC Oral Health, 2016, v. 16, article no. 70 | - |
dc.identifier.issn | 1472-6831 | - |
dc.identifier.uri | http://hdl.handle.net/10722/238630 | - |
dc.description.abstract | Background: Hypophosphatasia is a rare inherited disease derived from mutations in tissue non-specific alkaline phosphatase genes, with typical oral symptoms including short root anomaly and dysplasia of dentin or cementum. Case presentation: Two young female patients presented with short root anomaly with a history of premature loss of deciduous and/or permanent teeth. The laboratory and imaging investigations were performed. One case was diagnosed as odontohypophosphatasia concurrent with hyperthyroidism, the other was odontohypophosphatasia concurrent with multiple radicular cysts. Conclusion: This report presents two cases of odontohypophosphatasia, a rare disease which is difficult to be diagnosed, and highlights that the history of premature loss of deciduous and/or permanent teeth, oral manifestation and laboratory tests are crucial for clinical diagnosis. | - |
dc.language | eng | - |
dc.publisher | BioMed Central Ltd. The Journal's web site is located at http://www.biomedcentral.com/bmcoralhealth/ | - |
dc.relation.ispartof | BMC Oral Health | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Alkaline phosphatase | - |
dc.subject | Cone-beam computed tomography | - |
dc.subject | Dysplasia | - |
dc.subject | Hyperthyroidism | - |
dc.subject | Radicular cyst | - |
dc.subject | Short root anomaly | - |
dc.title | Current concepts in odontohypophosphatasia form of hypophosphatasia and report of two cases | - |
dc.type | Article | - |
dc.identifier.email | Su, Y: richsu@hku.hk | - |
dc.identifier.authority | Su, Y=rp01916 | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1186/s12903-016-0266-0 | - |
dc.identifier.pmid | 27531358 | - |
dc.identifier.pmcid | PMC4988024 | - |
dc.identifier.scopus | eid_2-s2.0-84982135093 | - |
dc.identifier.hkuros | 271159 | - |
dc.identifier.volume | 16 | - |
dc.identifier.spage | article no. 70 | - |
dc.identifier.epage | article no. 70 | - |
dc.identifier.isi | WOS:000381734000001 | - |
dc.publisher.place | United Kingdom | - |
dc.identifier.issnl | 1472-6831 | - |