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Cerebral creatine deficiency syndrome
rareCreatine 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.
- Identifiers
- MONDO:0000456 Orphanet:79172
- Also known as
- CCDS · CDS · creatine deficiency syndrome
Subtypes
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