Hypertryptophanaemia (Q89413): Difference between revisions
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A hipertriptofanemia familiar é caracterizada por deficiência intelectual associada a problemas comportamentais: mudanças periódicas de humor, respostas afetivas exageradas e comportamento sexual anormal. Doze casos foram relatados até agora. Anormalidades congênitas no metabolismo do triptofano parecem ser responsáveis pela triptofanemia e triptofanúria. | |||
| description / en | description / en | ||
Familial hypertryptophanaemia is characterised by intellectual deficit associated with behavioural problems: periodic mood swings, exaggerated affective responses and abnormal sexual behaviour. Twelve cases have been reported so far. Congenital abnormalities in tryptophan metabolism appear to be responsible for the tryptophanaemia and tryptophanuria. | |||
Revision as of 16:06, 15 August 2026
Familial hypertryptophanaemia is characterised by intellectual deficit associated with behavioural problems: periodic mood swings, exaggerated affective responses and abnormal sexual behaviour. Twelve cases have been reported so far. Congenital abnormalities in tryptophan metabolism appear to be responsible for the tryptophanaemia and tryptophanuria.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1215141359 |
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| English | Hypertryptophanaemia |
Familial hypertryptophanaemia is characterised by intellectual deficit associated with behavioural problems: periodic mood swings, exaggerated affective responses and abnormal sexual behaviour. Twelve cases have been reported so far. Congenital abnormalities in tryptophan metabolism appear to be responsible for the tryptophanaemia and tryptophanuria. |
