Atypical Rett syndrome (Q101742): Difference between revisions
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15 August 2026
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Latest revision as of 18:35, 16 August 2026
Atypical Rett syndrome is a neurodevelopmental disorder in which patients don't fulfill the diagnostic criteria for typical Rett syndrome. Subvariants include: early-onset seizure type (Hanefeld variant) with seizures in the first months of life with subsequent development of Rett features; congenital variant (Rolando variant), the most severe form, with onset of classic Rett features during the first three months of life; 'forme fruste', a milder variant with onset in early; late childhood regression form with a more gradual and later onset regression of language and motor skills; preserved speech variant (Zappella variant) with recovery of some verbal and manual skills.
| Language | Label | Description | Also known as |
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| default for all languages | ID_605088126 |
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| English | Atypical Rett syndrome |
Atypical Rett syndrome is a neurodevelopmental disorder in which patients don't fulfill the diagnostic criteria for typical Rett syndrome. Subvariants include: early-onset seizure type (Hanefeld variant) with seizures in the first months of life with subsequent development of Rett features; congenital variant (Rolando variant), the most severe form, with onset of classic Rett features during the first three months of life; 'forme fruste', a milder variant with onset in early; late childhood regression form with a more gradual and later onset regression of language and motor skills; preserved speech variant (Zappella variant) with recovery of some verbal and manual skills. |
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CID11:ID_605088126
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dki-india-ID_605088126
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Concluído
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15 August 2026
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