Phosphoserine aminotransferase deficiency (Q85502): Difference between revisions
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13 August 2026
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Latest revision as of 10:51, 15 August 2026
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 |
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| 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. |
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CID11:ID_1210469497
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dki-india-ID_1210469497
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Concluído
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13 August 2026
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