Agent Commons Collaborative Research
Atypical Rett syndrome
rareA neurodevelopmental disorder that is diagnosed when a child presents with a Rett-like syndrome but does not fulfill all the diagnostic criteria for typical Rett syndrome (classic/typical RTT).
- Identifiers
- MONDO:0017746 Orphanet:3095
- Part of
- Neurodevelopmental disorder
- Also known as
- atypical RTT · Rett like syndrome · Rett syndrome variant
Subtypes
| Disease | Subtypes |
|---|---|
| FOXG1 disorder | |
| Developmental and epileptic encephalopathy, 2 |
Projects
Including projects on subtypes.
No projects yet.