Prognostic Significance of Mutation Type and Chromosome Fragility in Fanconi Anemia

Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

Status: Completed

Conditions: Fanconi Anemia

Study type: Observational

Funder types: Other

Identifiers

NCT06490510

IIBSP-PFA-2024-47

Details and patient eligibility

About

The goal of this observational study is to analyze the data included in the Spanish Registry of Patients with Fanconi anemia to better understand the natural history of the disease, identify genetic risk and prognostic factors, and identify potential therapeutic strategies.

Enrollment: 227 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• All patients in the Spanish Registry of Patients with Fanconi Anemia

Exclusion criteria