Hypertryptophanaemia (Q89413): Difference between revisions

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Latest 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
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.