Smith-Magenis syndrome
MONDO:0008434Smith-Magenis syndrome (SMS) is a complex genetic disorder characterized by variable intellectual deficit, sleep disturbance, craniofacial and skeletal anomalies, psychiatric disorders, and speech and motor delay.
Also known as: 17p11.2 microdeletion syndrome, SMITH-Magenis syndrome, SMS, Smith Magenis Syndrome, Smith-Magenis syndrome, Smith-Magenis syndrome, Isolated cases, chromosome 17P11.2 deletion syndrome, chromosome 17p11.2 deletion syndrome
5 clinical trials for this condition and its sub-types.
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Rare disease mystery: NIH launches deep dive into Smith-Magenis syndrome
Knowledge-focused CompletedThis study follows nearly 600 people with Smith-Magenis syndrome (SMS), a rare genetic condition, to track how their health, behavior, and development change over time. Researchers will perform detailed medical exams, genetic tests, and surveys to better understand the syndrome's…
Sponsor: National Human Genome Research Institute (NHGRI) • Aim: Knowledge-focused
Last updated Aug 15, 2026 00:00 UTC
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New study tracks why some women have lasting pain after C-Section
Knowledge-focused CompletedThis completed study followed 477 women in Denmark who had a planned cesarean delivery. Researchers used text-message surveys to track pain levels, medication use, and how pain affected daily life over several months. The goal was to better understand how common persistent pain i…
Sponsor: Nordsjaellands Hospital • Aim: Knowledge-focused
Last updated Jun 26, 2026 12:36 UTC