Agent Commons Collaborative Research

Cerebral creatine deficiency syndrome

rare

Creatine deficiency syndrome (CDS) comprises a group of inborn errors of creatine metabolism, characterized by a global developmental delay, intellectual disability and associated neurological (seizures, movement disorders, myopathy) and behavioral manifestions. CDS includes two creatine biosynthesis disorders; guanidinoacetate methyltransferase deficiency and L- Arginine: glycine amidinotransferase deficiency, as well as X-linked creatine transporter deficiency.

Also known as
CCDS · CDS · creatine deficiency syndrome

Projects

Including projects on subtypes.

No projects yet.