Secondary neurodevelopmental syndrome (Q61621): Difference between revisions
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Síndrome que envolve características significativas do neurodesenvolvimento, e que não preenche critérios diagnósticos de nenhum transtorno do neurodesenvolvimento específico, e considerada consequência fisiopatológica direta de uma condição de saúde não classificada como transtorno mental e comportamental (p. ex., características que se assemelham ao autismo na síndrome de Rett; agressão e automutilação na síndrome de Lesch-Nyhan, anormalidades no desenvolvimento da linguagem na síndrome de Williams) com base em evidências de anamnese, exame físico ou achados laboratoriais. _x000D_ _x000D_ Essa categoria deve ser utilizada somada ao diagnóstico do transtorno ou doença subjacente presumido, quando problemas do neurodesenvolvimento são suficientemente graves para exigir atenção clínica específica. | |||
| description / en | description / en | ||
A syndrome that involves significant neurodevelopmental features that do not fulfill the diagnostic requirements of any of the specific neurodevelopmental disorders that is judged to be a direct pathophysiological consequence of a health condition not classified under mental and behavioural disorders (e.g., autistic-like features in Rett syndrome; aggression and self-mutilation in Lesch-Nyhan syndrome, abnormalities in language development in Williams syndrome), based on evidence from the history, physical examination, or laboratory findings. This category should be used in addition to the diagnosis for the presumed underlying disorder or disease when the neurodevelopmental problems are sufficiently severe to warrant specific clinical attention. | |||
Revision as of 09:06, 14 August 2026
A syndrome that involves significant neurodevelopmental features that do not fulfill the diagnostic requirements of any of the specific neurodevelopmental disorders that is judged to be a direct pathophysiological consequence of a health condition not classified under mental and behavioural disorders (e.g., autistic-like features in Rett syndrome; aggression and self-mutilation in Lesch-Nyhan syndrome, abnormalities in language development in Williams syndrome), based on evidence from the history, physical examination, or laboratory findings. This category should be used in addition to the diagnosis for the presumed underlying disorder or disease when the neurodevelopmental problems are sufficiently severe to warrant specific clinical attention.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 5999999999999999696322811782444113201781870066080460438503424 |
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| English | Secondary neurodevelopmental syndrome |
A syndrome that involves significant neurodevelopmental features that do not fulfill the diagnostic requirements of any of the specific neurodevelopmental disorders that is judged to be a direct pathophysiological consequence of a health condition not classified under mental and behavioural disorders (e.g., autistic-like features in Rett syndrome; aggression and self-mutilation in Lesch-Nyhan syndrome, abnormalities in language development in Williams syndrome), based on evidence from the history, physical examination, or laboratory findings. This category should be used in addition to the diagnosis for the presumed underlying disorder or disease when the neurodevelopmental problems are sufficiently severe to warrant specific clinical attention. |
