Phosphoserine aminotransferase deficiency (Q85502)

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

Language	Label	Description	Also known as
default for all languages	ID_1210469497
English	Phosphoserine aminotransferase deficiency	Phosphoserine aminotransferase deficiency is an extremely rare form of serine deficiency syndrome characterised clinically in the two reported cases to date by acquired microcephaly, psychomotor retardation, intractable seizures and hypertonia.