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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