Cure My Disease

Don't miss your cure!

Home News Browse Soon ready About
Log in / Sign up

Smith-Lemli-Opitz syndrome

MONDO:0010035

Smith-Lemli-Opitz syndrome (SLOS) is characterized by multiple congenital anomalies, intellectual deficit, and behavioral problems.

Also known as: 7-dehydrocholesterol reductase deficiency, RSH syndrome, Rutledge lethal multiple congenital anomaly syndrome, SLO syndrome, SLOS, Smith-Lemli-Opitz syndrome, Smith Lemli Opitz syndrome, lethal acrodysgenital syndrome

6 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Disease (680) Metabolic disease (233) Inherited lipid metabolism disorder (189) Hereditary disease (176) Eye disorder (102) Inborn errors of metabolism (45) Syndromic disease (25) Human disease (14) Developmental defect during embryogenesis (8) Cholesterol metabolism disease (3)
Trials to join now! 1 Not yet finished but already full! 2 Completed 2 Terminated 1
Sort by
  • Scientists dive into rare cholesterol disorders to uncover clues

    Knowledge-focused Terminated

    This study looks at rare genetic disorders where the body can't make cholesterol properly, which can cause birth defects and learning problems. Researchers collect blood, urine, and tissue samples from affected people and their families to learn more about these conditions. The g…

    Sponsor: Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) • Aim: Knowledge-focused

    Last updated Aug 14, 2026 00:00 UTC

Cure My Disease

Helping patients find clinical trials that match their disease.

Why was Cure my disease built?

Explore

Home News Browse About Terms of use Contact us

This is a site from Cyber and Space