Early infantile epileptic encephalopathy with suppression bursts

disorder

SNOMED 230429005CUI C0393706

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Epilepsy

Always present (100%)HP:0001250

Epileptic encephalopathy

Very frequent (80-99%)HP:0200134

Generalized myoclonic seizure

Very frequent (80-99%)HP:0002123

Localized motor seizures

Very frequent (80-99%)HP:0011153

Low intelligence

Very frequent (80-99%)HP:0001249

Psychomotor development deficiency

Very frequent (80-99%)HP:0001263

Deglutition disorder

Frequent (30-79%)HP:0002015

Delay in head control

Frequent (30-79%)HP:0002421

EEG with burst suppression

Frequent (30-79%)HP:0010851

Electroencephalogram abnormal

Frequent (30-79%)HP:0002353

Feeding difficulties

Frequent (30-79%)HP:0011968

Focal tonic seizure

Frequent (30-79%)HP:0011167

Hypotonia, early

Frequent (30-79%)HP:0008947

Hypsarrhythmia by EEG

Frequent (30-79%)HP:0002521

Inactivity

Frequent (30-79%)HP:0001254

Increased reflexes

Frequent (30-79%)HP:0001347

Poor sucking

Frequent (30-79%)HP:0002033

respiratory infections, recurrent

Frequent (30-79%)HP:0002205

Trouble sleeping

Frequent (30-79%)HP:0002360

Autism spectrum disorder

Occasional (5-29%)HP:0000729

Autoagression

Occasional (5-29%)HP:0100716

Cerebral pachygyria

Occasional (5-29%)HP:0001302

Choreoathetosis

Occasional (5-29%)HP:0001266

Delayed myelination

Occasional (5-29%)HP:0012448

Diffuse cerebral atrophy

Occasional (5-29%)HP:0002506

Diffuse white matter abnormalities

Occasional (5-29%)HP:0007204

Dyskinesia

Occasional (5-29%)HP:0100660

EEG with spike-wave complexes

Occasional (5-29%)HP:0010850

Febrile seizure (within the age range of 3 months to 6 years)

Occasional (5-29%)HP:0002373

Focal seizures

Occasional (5-29%)HP:0007359

Related Conditions

Early-infantile developmental and epileptic encephalopathy(parent)

Quick Facts

SNOMED CT: 230429005
UMLS CUI: C0393706
Fully Specified Name: Early infantile epileptic encephalopathy with suppression bursts (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 30

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.