Growth of kids with inborn metabolism disorders
Part of Genetic & congenital, Hormones & metabolism clinical trials.
This study looks at how children with certain rare metabolic disorders grow and develop. It may help doctors better understand these conditions and how to support affected children.
Summary written for real people, not researchers, by Clin2.
Who can take part
- Your child must be under 5 years old.
- Your child must have a confirmed diagnosis of an inborn error of metabolism.
- Your child must be seen at the study sites in Assiut Governorate.
- Your child must not have any major physical differences or birth defects diagnosed since birth.
- Your child must not have other brain or nerve problems like cerebral palsy, seizures, or lack of oxygen at birth.
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 study tests a targeted approach to help teenagers with inherited metabolism conditions successfully transfer from children’s to adult healthcare. It may help families feel more confident and reduce problems during the handoff to adult services.
This study looks at specific molecules in blood and breath to better understand metabolic conditions. It may help find new ways to monitor these conditions without invasive tests.
This study uses a simple blood spot and urine test to look for chemical signs of rare metabolic diseases. It aims to improve early detection and understanding of these conditions across all ages, including healthy individuals.
This research study follows patients with methylmalonic acidemia (a rare metabolic disorder affecting how the body breaks down certain proteins) or cobalamin (vitamin B12) disorders to better understand how these conditions develop and progress over time. Researchers will collect medical information, blood samples, and eye exams to help improve future treatments.
This study looks at which skin problems are common in children with inborn errors of immunity (immune system disorders from birth). It aims to help doctors better recognize and treat these skin issues.
This study looks at children who may have genetic (inherited) or metabolic (body chemistry) problems, including newborn screening and episodes of trouble. The goal is to better understand these conditions and identify children who may benefit from further care.
Hear when a new Inborn Errors of Metabolism trial opens
We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.