The Cute Syndrome Foundation | Genetic and Rare Diseases Information Center (GARD)

Supported Diseases

PCDH19-related female-limited epilepsy

Synonyms: EFMR, Female restricted epilepsy with intellectual disability, Epileptic encephalopathy, early infantile, 9, EIEE9, Juberg-Hellman syndrome, PCDH19-related FLE, PCDH19-related infantile epileptic encephalopathy

SCN8A encephalopathy

Synonyms: Early infantile epileptic encephalopathy-13, Epileptic Encephalopathy, early infantile, 13, EIEE13, SCN8A epilepsy

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