Molekulargenetisches Labor
Zentrum für Nephrologie und Stoffwechsel
Die autosomal dominante Zahnbildungsstörung wird durch Mutationen im PTHR1-Gen hervorgerufen. Die verschiedenen Dentifikationsstörungen führen meist zu einer asymmetrischen Hypodontie.
| 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
|
 |
Copyright © 2005-2020 Zentrum für Nephrologie und Stoffwechsel, Dr. Mato Nagel Albert-Schweitzer-Ring 32, D-02943 Weißwasser, Deutschland, Tel.: +49-3576-287922, Fax: +49-3576-287944 Seitenüberblick | Webmail | Haftungsausschluss | Datenschutz |
