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PSAT deficiency
rarePhosphoserine 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.
- Identifiers
- MONDO:0012596 OMIM:610992Orphanet:284417
- Causal genes
- PSAT1
- Also known as
- phosphoserine aminotransferase deficiency · PSATD
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