Axenfeld-Rieger syndrome: orthopedic and orthodontic management in a pediatric patient: a case report.
Head Face Med
; 18(1): 25, 2022 Jul 08.
Article
en En
| MEDLINE
| ID: mdl-35804381
ABSTRACT
Axenfeld-Rieger Syndrome (ARS) is a rare autosomal dominant genetic disease with considerable expressive variability, characterized by ocular and non-ocular manifestations, cardiovascular, mild craniofacial abnormalities and dental malformations. Current data report an incidence of Xenfeld-Rieger syndrome in the population of 1 200,000.The case described is that of a 14-year-old female patient whose ARS is suspected and investigated following a dental specialist visit for orthodontic reasons, acquired the patient's family and clinical data following a medical approach multidisciplinary, we proceed to the orthodontic involved the use of the Rapid Palatal Expander (RPE) and a fixed orthodontic treatment.The aim of this study is to report the case of the orthopaedic and orthodontic treatment in a patient affected by ARS and with facial dysmorphism and teeth anomalies associated to ocular anomalies.
Palabras clave
Texto completo:
1
Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Ortopedia
/
Enfermedades Hereditarias del Ojo
/
Anomalías del Ojo
Límite:
Adolescent
/
Child
/
Female
/
Humans
Idioma:
En
Revista:
Head Face Med
Asunto de la revista:
MEDICINA
/
ODONTOLOGIA
/
ORTOPEDIA
Año:
2022
Tipo del documento:
Article
País de afiliación:
Italia