Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 51 - 60 of 70 for Childhood epilepsy
  1. CLN8 disease 
    ... in this form involve uncontrollable muscle jerks (myoclonic epilepsy). ... survive only into late childhood or adolescence.CLN8 disease is one of a ...
    https://medlineplus.gov/genetics/condition/cln8-disease - Genetics
  2. CLN2 disease 
    ... 4. The initial features usually include recurrent seizures (epilepsy) and ... wheelchair by late childhood and typically do not survive past their teens. ...
    https://medlineplus.gov/genetics/condition/cln2-disease - Genetics
  3. Partington syndrome 
    ... that affect communication and social interaction. Recurrent seizures (epilepsy) may also occur in Partington syndrome.Focal dystonia ... in familial cases of mental retardation with infantile epilepsy and/or hand dystonia. Am J Med Genet ...
    https://medlineplus.gov/genetics/condition/partington-syndrome - Genetics
  4. CLPB deficiency 
    ... hypertonia), swallowing problems, difficulty breathing, and recurrent seizures (epilepsy). These babies may also have movement abnormalities, such ... abnormalities. Other features of moderate CLPB deficiency include epilepsy and mild to severe intellectual disability. Neutropenia in ...
    https://medlineplus.gov/genetics/condition/clpb-deficiency - Genetics
  5. Permanent neonatal diabetes mellitus 
    ... neurological problems, including developmental delay and recurrent seizures (epilepsy). This combination of developmental delay, epilepsy, and neonatal ...
    https://medlineplus.gov/.../permanent-neonatal-diabetes-mellitus - Genetics
  6. Spinal muscular atrophy 
    ... such as spinal muscular atrophy with progressive myoclonic epilepsy, spinal muscular atrophy with lower extremity predominance, X- ... atrophy type I do not survive past early childhood due to respiratory failure.Spinal muscular atrophy type ...
    https://medlineplus.gov/genetics/condition/spinal-muscular-atrophy - Genetics
  7. Timothy syndrome 
    ... deficit/hyperactivity disorder, intellectual disability and recurrent seizures (epilepsy); some affected individuals have photosensitive epilepsy, in which ...
    https://medlineplus.gov/genetics/condition/timothy-syndrome - Genetics
  8. Episodic ataxia 
    ... subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia. Am J Hum Genet. 2000 ... in the sodium channel gene SCN2A cause neonatal epilepsy with late-onset episodic ataxia. J Neurol. 2016 ...
    https://medlineplus.gov/genetics/condition/episodic-ataxia - Genetics
  9. TRNT1 deficiency 
    ... the inner ear (sensorineural hearing loss), recurrent seizures (epilepsy), and problems with the kidneys or heart.TRNT1 ... and affected individuals usually do not survive past childhood. RPEM, on the other hand, is recognized in ...
    https://medlineplus.gov/genetics/condition/trnt1-deficiency - Genetics
  10. Familial paroxysmal kinesigenic dyskinesia 
    ... to genetic linkage with benign familial infantile convulsions. Epilepsy Res. 2006 Aug;70 Suppl 1:S174-84. ... AJ, Houlden H, Kurian MA. Clinical features of childhood-onset paroxysmal kinesigenic dyskinesia with PRRT2 gene mutations. ...
    https://medlineplus.gov/...amilial-paroxysmal-kinesigenic-dyskinesia - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · next