Idiopathic Gingival Hyperplasia: A Case Report with a 17-Year Followup

This is a case report of a patient with idiopathic gingival hyperplasia and an undiagnosed genetic disorder that demonstrated static encephalopathy, mental retardation, developmental delay, seizures, hypotonia, and severe gingival hypertrophy. The clinical dental management and attempts to obtain a...

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Main Authors: Bien Lai, Joseph Muenzer, Michael W. Roberts
Format: Article
Language:English
Published: Wiley 2011-01-01
Series:Case Reports in Dentistry
Online Access:http://dx.doi.org/10.1155/2011/986237
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author Bien Lai
Joseph Muenzer
Michael W. Roberts
author_facet Bien Lai
Joseph Muenzer
Michael W. Roberts
author_sort Bien Lai
collection DOAJ
description This is a case report of a patient with idiopathic gingival hyperplasia and an undiagnosed genetic disorder that demonstrated static encephalopathy, mental retardation, developmental delay, seizures, hypotonia, and severe gingival hypertrophy. The clinical dental management and attempts to obtain a genetic diagnosis are described.
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institution Kabale University
issn 2090-6447
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publishDate 2011-01-01
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series Case Reports in Dentistry
spelling doaj-art-fcc6a7e26b4b45a697d13d61c91abdfb2025-02-03T00:58:56ZengWileyCase Reports in Dentistry2090-64472090-64552011-01-01201110.1155/2011/986237986237Idiopathic Gingival Hyperplasia: A Case Report with a 17-Year FollowupBien Lai0Joseph Muenzer1Michael W. Roberts2Department of Pediatric Dentistry, CB 7450, School of Dentistry, University of North Carolina, Chapel Hill, NC 27599-7450, USADivision of Pediatric Genetics and Metabolism, Department of Pediatrics, CB 7484, School of Medicine, University of North Carolina, Chapel Hill, NC, USADepartment of Pediatric Dentistry, CB 7450, School of Dentistry, University of North Carolina, Chapel Hill, NC 27599-7450, USAThis is a case report of a patient with idiopathic gingival hyperplasia and an undiagnosed genetic disorder that demonstrated static encephalopathy, mental retardation, developmental delay, seizures, hypotonia, and severe gingival hypertrophy. The clinical dental management and attempts to obtain a genetic diagnosis are described.http://dx.doi.org/10.1155/2011/986237
spellingShingle Bien Lai
Joseph Muenzer
Michael W. Roberts
Idiopathic Gingival Hyperplasia: A Case Report with a 17-Year Followup
Case Reports in Dentistry
title Idiopathic Gingival Hyperplasia: A Case Report with a 17-Year Followup
title_full Idiopathic Gingival Hyperplasia: A Case Report with a 17-Year Followup
title_fullStr Idiopathic Gingival Hyperplasia: A Case Report with a 17-Year Followup
title_full_unstemmed Idiopathic Gingival Hyperplasia: A Case Report with a 17-Year Followup
title_short Idiopathic Gingival Hyperplasia: A Case Report with a 17-Year Followup
title_sort idiopathic gingival hyperplasia a case report with a 17 year followup
url http://dx.doi.org/10.1155/2011/986237
work_keys_str_mv AT bienlai idiopathicgingivalhyperplasiaacasereportwitha17yearfollowup
AT josephmuenzer idiopathicgingivalhyperplasiaacasereportwitha17yearfollowup
AT michaelwroberts idiopathicgingivalhyperplasiaacasereportwitha17yearfollowup