Rett syndrome (Q40891): Difference between revisions
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Condição em que o desenvolvimento inicial aparentemente normal é seguido por perda parcial ou completa da fala e das habilidades de locomoção e uso das mãos, juntamente com desaceleração do crescimento da cabeça, geralmente com início entre sete e 24 meses de idade. Perda de movimentos intencionais das mãos, estereotipias de torcer as mãos e hiperventilação são características. O desenvolvimento social e lúdico é interrompido, mas o interesse social tende a ser mantido. Ataxia e apraxia do tronco começam a se desenvolver por volta dos quatro anos de idade e frequentemente são seguidos por movimentos coreoatetóticos. O resultado quase invariavelmente é um atraso intelectual grave. | |||
| description / en | description / en | ||
A condition in which apparently normal early development is followed by partial or complete loss of speech and of skills in locomotion and use of hands, together with deceleration in head growth, usually with an onset between seven and 24 months of age. Loss of purposive hand movements, hand-wringing stereotypies, and hyperventilation are characteristic. Social and play development are arrested but social interest tends to be maintained. Trunk ataxia and apraxia start to develop by age four years and choreoathetoid movements frequently follow. Severe mental retardation almost invariably results. | |||
Revision as of 06:54, 13 August 2026
A condition in which apparently normal early development is followed by partial or complete loss of speech and of skills in locomotion and use of hands, together with deceleration in head growth, usually with an onset between seven and 24 months of age. Loss of purposive hand movements, hand-wringing stereotypies, and hyperventilation are characteristic. Social and play development are arrested but social interest tends to be maintained. Trunk ataxia and apraxia start to develop by age four years and choreoathetoid movements frequently follow. Severe mental retardation almost invariably results.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD90.4 |
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| English | Rett syndrome |
A condition in which apparently normal early development is followed by partial or complete loss of speech and of skills in locomotion and use of hands, together with deceleration in head growth, usually with an onset between seven and 24 months of age. Loss of purposive hand movements, hand-wringing stereotypies, and hyperventilation are characteristic. Social and play development are arrested but social interest tends to be maintained. Trunk ataxia and apraxia start to develop by age four years and choreoathetoid movements frequently follow. Severe mental retardation almost invariably results. |
