Exploring Kleefstra syndrome cohort phenotype characteristics: Prevalence insights from caregiver-reported outcomes
Kleefstra syndrome (KLEFS1) is a rare genetic neurodevelopmental disorder affecting multiple body systems. It continues to be under-researched, and its prevalence remains unknown. This paper builds on the international KLEFS1 cohort of 172 individuals based on the caregiver-reported outcomes collected within the online data collection platform GenIDA and reports the occurrence, frequency and severity of symptoms in KLEFS1. The study clearly shows the importance of caregiver-reported outcomes collections in the rare disease domain. Moreover, the study emphasizes the need for more specific and enhanced data collection methods, suggesting recommendations to optimize caregiver-reported registries and foster an even more profound understanding of rare diseases.
Authors
- Arianne Bouman (ORCID: https://orcid.org/0000-0002-1138-8026)
- Pauline Burger (ORCID: https://orcid.org/0000-0003-2109-5451)
- Alenka Guček
- Tanja Zdolšek Draksler
- Florent Colin
- Tjitske Kleefstra (ORCID: https://orcid.org/0000-0002-0956-0237)
- Erik Novak
Institutions
- Radboud University Nijmegen (NL)
- Radboud University Medical Center (NL)
- Jožef Stefan Institute (SI)
- Institut de génétique et de biologie moléculaire et cellulaire (FR)
- Jožef Stefan International Postgraduate School (SI)
- Vincent Van Gogh Voor Geestelijke Gezondheidszorg (NL)
- Université de Strasbourg (FR)
Publication Details
- Journal
- European Journal of Medical Genetics
- Published
- 2024-09-17
- DOI
- https://doi.org/10.1016/j.ejmg.2024.104974
- Citations
- 7
- Primary Topic
- Epigenetics and DNA Methylation
- Type
- article
- Field-Weighted Citation Impact
- 1.64
Funders
- ZonMw
- Nederlandse Organisatie voor Wetenschappelijk Onderzoek