Status: Available
Rescue of Infants With MCT8 Deficiency
Monocarboxylate Transporter 8 (MCT8) deficiency (that is also known as Allan-Herndon-Dudley syndrome) is a rare X-linked inherited disorder of brain development that causes severe intellectual disability and problems with movement. This condition, which occurs almost exclusively in males, disrupts development from before birth.
Trial details
Age: Up to 18Biological sex: MaleType: Expanded AccessSponsor: Roy E. Weiss, M.D.Updated: Dec 11, 2025Locations: 1
Eligibility criteria
Genetic Confirmation: Male fetus or fetuses (including monozygotic twin pregnanc... [+4]
Atrial fibrillation or other arrhythmias. [+2]