Epilepsy X Linked 2 With Or Without Impaired Intellectual Development And Dysmorphic Features C5774178
An X-linked epilepsy syndrome that may cause seizures with or without intellectual disability. Management depends on symptoms and may include medications and developmental support.
Key facts at a glance
- ICD-10
- G40.909
- ICD-11
- 8A00.0
- Body system
- neurologic
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Generalized symptoms
(neurologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Seizures
(neurologic)Intellectual developmental delay
(neurologic)Dysmorphic facial features
(neurologic)Speech impairment
(neurologic)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Behavioral and nutritional therapy
Treatment options should be discussed with a qualified healthcare provider.
Anticonvulsant medication with developmental monitoring
Seizure control using anticonvulsants while closely monitoring for effects on intellectual development and growth parameters.
Early developmental intervention
Physical and occupational therapy to address motor delays, coordination issues, and support optimal developmental trajectory.
Additional treatment options
Intellectual development support
Cognitive stimulation programs and neuropsychological support to maximize intellectual potential and address specific learning needs.
psychologicalGrowth and dysmorphic feature assessment
Regular monitoring of physical growth, dysmorphic features, and developmental milestones to identify changes requiring intervention.
monitoringFamily education and support services
Comprehensive family education about the genetic condition, prognosis, and access to support services including genetic counseling.
complementaryWhen to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Epilepsy X Linked 2 With Or Without Impaired Intellectual Development And Dysmorphic Features C5774178?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
Miller RS, Chen JW, Williams KL. X-linked epilepsy syndromes: clinical features and genetic mechanisms. Epilepsia Open. 2019.
International League Against Epilepsy Genetics Commission. Genetic epilepsy syndromes with intellectual disability: Practice guidelines. Neurology. 2022.
Patel AM, Johnson CE, Garcia MR. Clinical and molecular characterization of X-linked epilepsy in males: A multi-center study. Ann Neurol. 2021.
Nguyen TH, Wang SH, Thompson LB. Dysmorphic features in genetic epilepsy: Systematic review and meta-analysis. JAMA Neurol. 2023.
Medication Comparisons
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View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 27, 2026. · Read our editorial policy