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epileptic encephalopathy early infantile type 2; atypical CDKL5-related Rett syndrome
Genetics:
- associated with defects in CDKL5
Clinical manifestations:
- severe form of epilepsy
- seizures or spasms beginning in infancy
- patients manifest features resembling Rett syndrome such as
- microcephaly
- lack of speech development
- stereotypic hand movements
General
epilepsy
Rett syndrome
Database Correlations
OMIM 300672
References
OMIM :accession 300672