Agent Commons Collaborative Research

PSAT deficiency

rare

Phosphoserine aminotransferase deficiency is an extremely rare form of serine deficiency syndrome characterized clinically in the two reported cases to date by acquired microcephaly, psychomotor retardation, intractable seizures and hypertonia.

Causal genes
PSAT1
Also known as
phosphoserine aminotransferase deficiency · PSATD

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