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Chromosome Xp21 deletion syndrome
MONDO:0010399Also known as: Del(X)(p21), Glycerol kinase deficiency-contiguous gene syndrome, Xp21 contiguous gene deletion syndrome, Xp21 microdeletion syndrome, chromosome Xp21 deletion syndrome, complex glycerol kinase deficiency, Complex Glycerol kinase deficiency
5 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
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New prenatal blood test aims to detect genetic disorders without invasive procedures
Diagnosis Recruiting nowThis study is testing a new blood test that looks for fetal cells in the mother's blood to detect genetic conditions like Down syndrome. The test will be compared to standard diagnostic methods such as amniocentesis or newborn testing. The study involves 1,000 pregnant individual…
Sponsor: BillionToOne Inc. • Aim: Diagnosis
Last updated Jun 27, 2026 13:06 UTC
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Social coaching may ease anxiety and autism traits in rare chromosome conditions
Symptom relief Recruiting nowThis trial tests whether a 10-session group program called Social Management Training can improve mental health, executive function, and social skills in adults aged 16 to 69 who have sex chromosome aneuploidies (extra or missing sex chromosomes). Participants complete questionna…
Phase: PHASE1 • Sponsor: University of Oslo • Aim: Symptom relief
Last updated Jul 24, 2026 00:00 UTC