MedPath

Clinical and genetic analysis of patients with primary failure of eruption (PFE) and their relatives

Conditions
K00.8
Other disorders of tooth development
Registration Number
DRKS00028019
Lead Sponsor
CharitéCentrum für Zahn-, Mund- und Kieferheilkunde CC 3
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
30
Inclusion Criteria

The patient must be at least 12 years of age, as an asymmetric eruption of the first permanent molars becomes evident (to avoid premature (incorrect) diagnosis of the eruption disorder). Gender does not matter, but must be specified for the evaluation of the genetic analysis.

The number of study participants:
Spirit. 10 trios with PFE (affected children of two phenotypically healthy or affected parents or affected family members)

Exclusion Criteria

Absence of an impacted tooth in the pretherapeutic orthopantomogram (root growth of the teeth that have not yet erupted is not complete).
Abnormal tooth germ position, tooth germ malformation, bone deficit in patients with clefts, dilaceration.
Syndromic and systemic diseases
Teeth that do not erupt due to lack of space.

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The aim of this study is to facilitate an easier clinical differential diagnosis of PFE, derive the causes of PFE in the genetic code through genetic analysis and localize the corresponding genes, to optimize or individualize the therapy of PFE based on the results of this study.<br><br>
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath