Hypertryptophanaemia (Q89413): Difference between revisions

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description / pt-brdescription / pt-br
 
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 / endescription / 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.
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Property / Canonical URI: https://id.who.int/icd/entity/1215141359 / rank
 
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Property / CURIE
 
CID11:ID_1215141359
Property / CURIE: CID11:ID_1215141359 / rank
 
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dki-india-ID_1215141359
Property / Canary Token: dki-india-ID_1215141359 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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Property / Collection date
 
13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 13 August 2026 / rank
 
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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.
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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
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      dki-india-ID_1215141359
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      Concluído
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      13 August 2026
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