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: | , , |
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| Format: | Book |
| Published: |
Hindawi Limited,
2011-01-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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| Summary: | 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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| Item Description: | 2090-6447 2090-6455 10.1155/2011/986237 |