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

Autor:	Jennie M, Waldron, Clare, McNamara, Antonia R, Hewson, C M, McNamara
Rok vydání:	2010
Předmět:	Pit and Fissure Sealants Cuspid Tooth Abnormalities Eye Diseases Hereditary Oral Hygiene Facial Bones Patient Care Planning Incisor Anterior Eye Segment Maxilla Denture Partial Removable Humans Bicuspid Female Nasal Bone Eye Abnormalities Child Anodontia Follow-Up Studies
Zdroj:	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. 30(5)
ISSN:	1754-4505
Popis:	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.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=pmid________::f38c476b002e1da209d02bdae371f87c https://pubmed.ncbi.nlm.nih.gov/20831741 Zobrazit plný text záznamu Plný text