developmental and epileptic encephalopathy, 24

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Disease Overview

Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the HCN1 gene.


Synonyms

  • DEE24
  • EIEE24
  • HCN1 early infantile epileptic encephalopathy
  • developmental and epileptic encephalopathy 24
  • early infantile epileptic encephalopathy caused by mutation in HCN1
  • epileptic encephalopathy, early infantile, 24
  • epileptic encephalopathy, early infantile, type 24

GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.

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National Organization for Rare Disorders