Platform to support genetic diagnosis in children
Part of Genetic & congenital clinical trials.
This trial is building a platform to help doctors diagnose rare genetic diseases in children. It asks neuropediatricians at a specific hospital to share their experience and help improve the process of referring kids to genetic specialists.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You work as a neuropediatrician at Carlos Van Buren Hospital.
- You care for children under 18 years old.
- You are a native Spanish speaker or have a C1-level certification in Spanish.
- You are the doctor who sends pediatric patients with suspected rare diseases to a genetics specialist.
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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