CHROMOSOME 17P13.3 MICRODELETION SYNDROME

Clinical trials for CHROMOSOME 17P13.3 MICRODELETION SYNDROME explained in plain language.

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New hope for families facing rare childhood illnesses

Symptom relief ENROLLING_BY_INVITATION

This study is testing a support program called FACE-Rare for families caring for children with serious, rare diseases. The program aims to help identify and meet families' needs for support, improve caregivers' quality of life, and assist with planning for future medical decision…

Matched conditions: CHROMOSOME 17P13.3 MICRODELETION SYNDROME

Phase: NA • Sponsor: Children's National Research Institute • Aim: Symptom relief

Last updated Mar 24, 2026 12:02 UTC

CHROMOSOME 17P13.3 MICRODELETION SYNDROME

Get alerted when new CHROMOSOME 17P13.3 MICRODELETION SYNDROME trials appear

New hope for families facing rare childhood illnesses