MEHMO syndrome: Understanding the condition over time
Part of Bones, joints & muscles, Brain & nervous system, Genetic & congenital, Hormones & metabolism, Mental health clinical trials.
This study follows people with or at risk for MEHMO syndrome over time to better understand the condition and identify biological markers. It may include both affected individuals and their family members to see how the condition runs in families.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You can be as young as 1 week old (if affected) or at least 1 month old (if not affected).
- You may join if you have signs or symptoms that suggest MEHMO syndrome and your genetic test results are not clear.
- You may also join if you are a relative of someone with MEHMO or a related condition, even if you don't have symptoms.
- People with a known MEHMO-related gene change, or those who are carriers of a family variant, can take part.
- You can also take part if you are a healthy family member without the genetic change.
- You cannot join if you have other medical issues that the study doctors think would make participation unsafe.
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
Similar studies
Other trials that look related to this one.
This trial uses genetic testing to find the cause of suspected metabolic diseases, including some cases of epilepsy. It may help you get a clearer diagnosis and guide treatment.
This study looks at a rare immune system condition caused by changes in the MOESIN gene. It aims to better understand the condition and may help develop future treatments.
This study follows adults with suspected or confirmed melorheostosis to understand how the condition develops and what outcomes to expect. It may help researchers better understand the disease and its genetic factors.
This study follows people with rare genetic conditions (GM1, GM2, sialidosis, or galactosialidosis) that affect how the body breaks down certain substances in cells. Researchers track how these diseases progress to better understand them and potentially help future patients.
This natural history study follows children and adults with suspected or confirmed mitochondrial myopathy to better understand symptoms and how the condition changes. It may also include healthy participants to compare test results and improve future treatments.
This study looks at how metabolism, infections, and the immune system work together in people with mitochondrial disease. It aims to learn more about the condition and may help guide future treatments.
Hear when a new Intellectual Disability trial opens
We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.