| Floating-Harbor syndrome: case report and craniofacial phenotype characterization. | |
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MedLine Citation:
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PMID: 15139957 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Floating-Harbor syndrome is a rare genetic disorder of unknown aetiology. It was described for the first time in 1973. The syndrome is characterized mainly by short stature, delay in speech development and characteristic facial features. This article describes a report of a case of the syndrome and emphasizes the oral aspects, including descriptions of soft tissues, teeth, occlusion, stage of dental development and findings on examination of the temporomandibular joint. The treatment provided and its outcome is also described. Hopefully this information will be compared with findings from other patients in the future to assist in clarifying the phenotype of the Floating-Harbor syndrome. |
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Authors:
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M S De Benedetto; F M Mendes; S Hirata; R O Guaré; A S Haddad; A L Ciamponi |
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Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: International journal of paediatric dentistry / the British Paedodontic Society [and] the International Association of Dentistry for Children Volume: 14 ISSN: 0960-7439 ISO Abbreviation: Int J Paediatr Dent Publication Date: 2004 May |
Date Detail:
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Created Date: 2004-05-13 Completed Date: 2004-07-06 Revised Date: 2004-11-17 |
Medline Journal Info:
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Nlm Unique ID: 9107511 Medline TA: Int J Paediatr Dent Country: England |
Other Details:
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Languages: eng Pagination: 208-13 Citation Subset: D |
Affiliation:
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Dental School, University of São Paulo, Brazil. niquesdb@hotmail.com |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Child Craniofacial Abnormalities / pathology Dwarfism / pathology* Facies* Humans Male Malocclusion / pathology Mouth / pathology Phenotype Speech Disorders / pathology* Syndrome Temporomandibular Joint / pathology Tooth Eruption / physiology |
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