ARTICLE: Axenfeld–Rieger Syndrome (ARS): A review and case report
Identifieur interne : 005464 ( Main/Curation ); précédent : 005463; suivant : 005465ARTICLE: Axenfeld–Rieger Syndrome (ARS): A review and case report
Auteurs : Jennie M. Waldron [Irlande (pays)] ; Clare Mcnamara [Royaume-Uni] ; Antonia R. Hewson [Irlande (pays)] ; C. M. Mcnamara [Irlande (pays)]Source :
- Special Care in Dentistry [ 0275-1879 ] ; 2010-09.
English descriptors
- KwdEn :
- Abnormality, Anomaly, Anterior chamber, Axenfeld syndrome, Bone density, Case report, Community services, Craniofacial, Craniofacial features, Dental anomalies, Dental department, Dental literature, Dental management, Dietary advice, Family history, First molar, Gingival maturation, Hypodontia, Hypoplasia, Incisor, Little information, Mandibular, Mandibular teeth, Maxillary, Maxillary hypodontia, Midface hypoplasia, Molar, Multidisciplinary approach, Neural crest cells, Ocular, Ocular features, Orthodontic treatment, Osteopenia, Osteoporosis, Partial denture, Periodontal disease, Periumbilical skin, Restorative care, Rieger syndrome, Secondary teeth, Somatic anomalies, Syndrome, Wide variety.
- Teeft :
- Abnormality, Anomaly, Anterior chamber, Axenfeld syndrome, Bone density, Case report, Community services, Craniofacial, Craniofacial features, Dental anomalies, Dental department, Dental literature, Dental management, Dietary advice, Family history, First molar, Gingival maturation, Hypodontia, Hypoplasia, Incisor, Little information, Mandibular, Mandibular teeth, Maxillary, Maxillary hypodontia, Midface hypoplasia, Molar, Multidisciplinary approach, Neural crest cells, Ocular, Ocular features, Orthodontic treatment, Osteopenia, Osteoporosis, Partial denture, Periodontal disease, Periumbilical skin, Restorative care, Rieger syndrome, Secondary teeth, Somatic anomalies, Syndrome, Wide variety.
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.
Url:
DOI: 10.1111/j.1754-4505.2010.00153.x
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ISTEX:19B54ABF9FCB8E102A14D8121D5A5598C0285A67Le document en format XML
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<term>Anomaly</term>
<term>Anterior chamber</term>
<term>Axenfeld syndrome</term>
<term>Bone density</term>
<term>Case report</term>
<term>Community services</term>
<term>Craniofacial</term>
<term>Craniofacial features</term>
<term>Dental anomalies</term>
<term>Dental department</term>
<term>Dental literature</term>
<term>Dental management</term>
<term>Dietary advice</term>
<term>Family history</term>
<term>First molar</term>
<term>Gingival maturation</term>
<term>Hypodontia</term>
<term>Hypoplasia</term>
<term>Incisor</term>
<term>Little information</term>
<term>Mandibular</term>
<term>Mandibular teeth</term>
<term>Maxillary</term>
<term>Maxillary hypodontia</term>
<term>Midface hypoplasia</term>
<term>Molar</term>
<term>Multidisciplinary approach</term>
<term>Neural crest cells</term>
<term>Ocular</term>
<term>Ocular features</term>
<term>Orthodontic treatment</term>
<term>Osteopenia</term>
<term>Osteoporosis</term>
<term>Partial denture</term>
<term>Periodontal disease</term>
<term>Periumbilical skin</term>
<term>Restorative care</term>
<term>Rieger syndrome</term>
<term>Secondary teeth</term>
<term>Somatic anomalies</term>
<term>Syndrome</term>
<term>Wide variety</term>
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<term>Case report</term>
<term>Community services</term>
<term>Craniofacial</term>
<term>Craniofacial features</term>
<term>Dental anomalies</term>
<term>Dental department</term>
<term>Dental literature</term>
<term>Dental management</term>
<term>Dietary advice</term>
<term>Family history</term>
<term>First molar</term>
<term>Gingival maturation</term>
<term>Hypodontia</term>
<term>Hypoplasia</term>
<term>Incisor</term>
<term>Little information</term>
<term>Mandibular</term>
<term>Mandibular teeth</term>
<term>Maxillary</term>
<term>Maxillary hypodontia</term>
<term>Midface hypoplasia</term>
<term>Molar</term>
<term>Multidisciplinary approach</term>
<term>Neural crest cells</term>
<term>Ocular</term>
<term>Ocular features</term>
<term>Orthodontic treatment</term>
<term>Osteopenia</term>
<term>Osteoporosis</term>
<term>Partial denture</term>
<term>Periodontal disease</term>
<term>Periumbilical skin</term>
<term>Restorative care</term>
<term>Rieger syndrome</term>
<term>Secondary teeth</term>
<term>Somatic anomalies</term>
<term>Syndrome</term>
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<front><div type="abstract" xml:lang="en">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.</div>
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