Hypertryptophanaemia (Q89413): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Verification Status | |||
Concluído | |||
| Property / Verification Status: Concluído / rank | |||
Normal rank | |||
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. |
Statements
CID11:ID_1215141359
0 references
dki-india-ID_1215141359
0 references
Concluído
0 references
