Zahnbildungsstörungen
Die autosomal dominante Zahnbildungsstörung wird durch Mutationen im PTHR1-Gen hervorgerufen. Die verschiedenen Dentifikationsstörungen führen meist zu einer asymmetrischen Hypodontie.
Gliederung
Referenzen:
| 1. |
Decker E et al. (2008) PTHR1 loss-of-function mutations in familial, nonsyndromic primary failure of tooth eruption. [^] |
| 2. |
Bosker H et al. (1978) Familial reinclusion of permanent molars. [^] |
| 3. |
Bianchi SD et al. (1991) Primary impaction of primary teeth: a review and report of three cases. [^] |
| 4. |
None (1974) Complete failure of eruption of all permanent teeth: an autosomal dominant disorder. [^] |
| 5. |
Proffit WR et al. (1981) Primary failure of eruption: a possible cause of posterior open-bite. [^] |
| 6. |
O'Connell AC et al. (1999) Primary failure of tooth eruption: a unique case. [^] |
| 7. |
Dibiase AT et al. (2000) Primary failure of eruption in the permanent dentition of siblings. [^] |
| 8. |
Ahmad S et al. (2006) The clinical features and aetiological basis of primary eruption failure. [^] |
| 9. |
Frazier-Bowers SA et al. (2007) Primary failure of eruption: further characterization of a rare eruption disorder. [^] |
| 10. |
OMIM.ORG article Omim 125350 [^] |
