Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome

disorder

SNOMED 1231737000CUI C1842531

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.

Localized motor seizures

Always present (100%)HP:0011153

tremors in hands

Very frequent (80-99%)HP:0002378

Difficulty articulating speech

Frequent (30-79%)HP:0001260

EEG with parietal focal spike waves

Frequent (30-79%)HP:0012012

EEG with parietal sharp waves

Frequent (30-79%)HP:0011295

Episodic dystonia

Frequent (30-79%)HP:0002268

Focal hemifacial clonic seizure

Frequent (30-79%)HP:0007332

Involuntary, rapid, rhythmic eye movements

Frequent (30-79%)HP:0000639

Writer's cramp

Frequent (30-79%)HP:0002356

Generalized tonic-clonic seizure (without specification of onset)

Occasional (5-29%)HP:0002069

Seizures

Occasional (5-29%)HP:0001250

Horizontal nystagmus

HP:0000666

Involuntary jerking movements

HP:0001336

Prolonged somatosensory evoked potentials

HP:0007104

Related Conditions

Hereditary disorder of nervous system(parent)

Benign Rolandic epilepsy(parent)

Recessive hereditary disorder (autosomal)(parent)

Paroxysmal dystonia(parent)

Quick Facts

SNOMED CT: 1231737000
UMLS CUI: C1842531
Fully Specified Name: Rolandic epilepsy, paroxysmal exercise-induced dystonia, writer's cramp syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 14

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.