6-pyruvoyl-tetrahydropterin synthase deficiency (Q105034): Difference between revisions
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16 August 2026
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Latest revision as of 10:56, 17 August 2026
6-pyruvoyl-tetrahydropterin synthase (PTPS) deficiency is one of the causes of malignant hyperphenylalaninemia due to tetrahydrobiopterin deficiency, as well as of defective neurotransmission of monoamines. When left untreated, the deficiency causes neurological signs at age 4 or 5 months including psychomotor retardation, tonus disorders, convulsions, drowsiness, irritability, abnormal movements, hyperthermia, hypersalivation and difficulty swallowing.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1744398760 |
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| English | 6-pyruvoyl-tetrahydropterin synthase deficiency |
6-pyruvoyl-tetrahydropterin synthase (PTPS) deficiency is one of the causes of malignant hyperphenylalaninemia due to tetrahydrobiopterin deficiency, as well as of defective neurotransmission of monoamines. When left untreated, the deficiency causes neurological signs at age 4 or 5 months including psychomotor retardation, tonus disorders, convulsions, drowsiness, irritability, abnormal movements, hyperthermia, hypersalivation and difficulty swallowing. |
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CID11:ID_1744398760
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dki-india-ID_1744398760
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Concluído
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16 August 2026
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