Синдром дефіциту креатину
ORPHA:79172· Creatine deficiency syndrome
Визначення(English summary)
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.
- Поширеність
- Unknown
- Успадкування
- Autosomal recessive, Not applicable, X-linked recessive
- Вік початку
- Childhood, Infancy