Axenfeld-Rieger syndrome (ARS): A review and case report.

Hdl Handle:
http://hdl.handle.net/10147/141032
Title:
Axenfeld-Rieger syndrome (ARS): A review and case report.
Authors:
Waldron, Jennie M; McNamara, Clare; Hewson, Antonia R; McNamara, C M
Affiliation:
Dental Department, Community Services, Mayo, Ireland.
Citation:
Axenfeld-Rieger syndrome (ARS): A review and case report., 30 (5):218-22 Spec Care Dentist
Journal:
Special care in dentistry : official publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry
Issue Date:
29-Aug-2011
URI:
http://hdl.handle.net/10147/141032
DOI:
10.1111/j.1754-4505.2010.00153.x
PubMed ID:
20831741
Additional Links:
http://www.ncbi.nlm.nih.gov/pubmed/20831741
Abstract:
Axenfeld-Rieger syndrome (ARS) is a rare, autosomal dominant condition characterized by ocular, craniofacial, dental, and periumbilical abnormalities. Relatively little information exists on this syndrome within the dental literature despite the fact that midface hypoplasia and maxillary hypodontia are classical presenting features of this syndrome. This is a case report of a 7-year-old Caucasian female with ARS who presented with significant ocular and dental anomalies. She was also found to have osteopenia. Her dental condition is described, her immediate treatment is shown, and her long-term treatment needs are discussed.
Item Type:
Article
Language:
en
MeSH:
Anodontia; Anterior Eye Segment; Bicuspid; Child; Cuspid; Denture, Partial, Removable; Eye Abnormalities; Facial Bones; Female; Follow-Up Studies; Humans; Incisor; Maxilla; Nasal Bone; Oral Hygiene; Patient Care Planning; Pit and Fissure Sealants; Tooth Abnormalities
ISSN:
1754-4505

Full metadata record

DC FieldValue Language
dc.contributor.authorWaldron, Jennie Men
dc.contributor.authorMcNamara, Clareen
dc.contributor.authorHewson, Antonia Ren
dc.contributor.authorMcNamara, C Men
dc.date.accessioned2011-08-29T09:11:03Z-
dc.date.available2011-08-29T09:11:03Z-
dc.date.issued2011-08-29T09:11:03Z-
dc.identifier.citationAxenfeld-Rieger syndrome (ARS): A review and case report., 30 (5):218-22 Spec Care Dentisten
dc.identifier.issn1754-4505-
dc.identifier.pmid20831741-
dc.identifier.doi10.1111/j.1754-4505.2010.00153.x-
dc.identifier.urihttp://hdl.handle.net/10147/141032-
dc.description.abstractAxenfeld-Rieger syndrome (ARS) is a rare, autosomal dominant condition characterized by ocular, craniofacial, dental, and periumbilical abnormalities. Relatively little information exists on this syndrome within the dental literature despite the fact that midface hypoplasia and maxillary hypodontia are classical presenting features of this syndrome. This is a case report of a 7-year-old Caucasian female with ARS who presented with significant ocular and dental anomalies. She was also found to have osteopenia. Her dental condition is described, her immediate treatment is shown, and her long-term treatment needs are discussed.-
dc.language.isoenen
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pubmed/20831741en
dc.subject.meshAnodontia-
dc.subject.meshAnterior Eye Segment-
dc.subject.meshBicuspid-
dc.subject.meshChild-
dc.subject.meshCuspid-
dc.subject.meshDenture, Partial, Removable-
dc.subject.meshEye Abnormalities-
dc.subject.meshFacial Bones-
dc.subject.meshFemale-
dc.subject.meshFollow-Up Studies-
dc.subject.meshHumans-
dc.subject.meshIncisor-
dc.subject.meshMaxilla-
dc.subject.meshNasal Bone-
dc.subject.meshOral Hygiene-
dc.subject.meshPatient Care Planning-
dc.subject.meshPit and Fissure Sealants-
dc.subject.meshTooth Abnormalities-
dc.titleAxenfeld-Rieger syndrome (ARS): A review and case report.en
dc.typeArticleen
dc.contributor.departmentDental Department, Community Services, Mayo, Ireland.en
dc.identifier.journalSpecial care in dentistry : official publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistryen

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