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Oligodontia phenotypes and their genetic pathways component

Oligodontia phenotypes and their genetic pathways component - Oli

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00027247
Enrollment
30
Registered
2022-06-07
Start date
2021-03-11
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Missing of 6 or more teeth.

Interventions

Group 1: 1) Blood sampling and genetic examination by the Genetics Institute. 2) Dental diagnosis

Sponsors

Charité Zahnklinik
Lead Sponsor

Eligibility

Sex/Gender
All
Age
9 Years to 99 Years

Inclusion criteria

Inclusion criteria: Absence of six or more permanent teeth (excluding wisdom teeth)

Exclusion criteria

Exclusion criteria: Younger than 9 years

Design outcomes

Primary

MeasureTime frame
1. The aim of the study is to investigate the appearance of patients with oligodontia. For this purpose, the numerical code (Tooth Agenesis Code, TAC) will be used to establish the correlation between the genotype and the phenotype of phenotype of the nongenesis. 2. the genetic material of the patients and their family members (adult siblings, parents or grandparents) will be analyzed according to the genes identified by previous studies. 3. in addition, new genes responsible for hypo /oligodontia (hypodontia: not attachment of 1-5 teeth, oligodontia: 6 or more unattached teeth). (hypodontia: 1-5 teeth not attached, oligodontia: 6 or more teeth not attached), using the whole genome sequencing method. 4. The purpose of the study is to standardize the diagnosis of patients with oligodontia.

Countries

Germany

Contacts

Public ContactJanna Mitscherling

Zahnklinik Charite

janna.mitscherling@gmx.de015203036890

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026