Oral abnormalities in the Ellis-van Creveld syndrome.
Article
Dans Anglais
| IMSEAR
| ID: sea-139825
ABSTRACT
Ellis-van Creveld (EvC) syndrome is an autosomal recessive disorder, mainly affecting the ectodermal components such as, enamel, nail, and hair. The gene for EvC syndrome is located on chromosome 4p16. Patients with EvC syndrome characteristically presents with congenitally missing teeth, abnormal frenal attachment, microdontia, and hexadactyly.
Texte intégral:
Disponible
Indice:
IMSEAR (Asie du Sud-Est)
Sujet Principal:
Malformations dentaires
/
Femelle
/
Humains
/
Syndrome d'Ellis-van Creveld
/
Adolescent
/
Consanguinité
/
Frein labial
/
Anodontie
langue:
Anglais
Année:
2010
Type:
Article
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