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Neurodevelopmental Disorder With Seizures And Nonepileptic Hyperkinetic Movements; NEDNEH

Disease ID:1281
Name:Neurodevelopmental Disorder With Seizures And Nonepileptic Hyperkinetic Movements; NEDNEH
Associated with:1 target
Database Links
OMIM: 618497

Targets

Cav2.2
Role:  A bi-allelic loss-of function has been reported in three unrelated families with different protein-truncating mutations. This resulted in an autosomal recessive, complex and progressive neurologic disorder with severe neurodevelopmental delay and developmental regression, drug-resistant epileptic encephalopathy, postnatal microcephaly, hypotonia, and a non-epileptic hyperkinetic movement disorder
References:  1

Ligands

No ligand related data available for Neurodevelopmental Disorder With Seizures And Nonepileptic Hyperkinetic Movements; NEDNEH

References

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1. Gorman KM, Meyer E, Grozeva D, Spinelli E, McTague A, Sanchis-Juan A, Carss KJ, Bryant E, Reich A, Schneider AL et al.. (2019) Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia. Am J Hum Genet, 104 (5): 948-956. [PMID:30982612]