Tbc1d24 Related Familial Infantile Myoclonic Epilepsy Fime Cn381258
A rare genetic epilepsy beginning in infancy, characterized by involuntary muscle jerks; managed with anti-seizure medications.
Key facts at a glance
- ICD-10
- G43.909
- 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
Myoclonic seizures
(neurologic)Focal seizures
(neurologic)Febrile seizures
(neurologic)Developmental delay
(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
Antiepileptic drug therapy
Seizure control through antiepileptic medications forms the cornerstone of FIME management, with selection based on seizure type and tolerability profile.
Exercise prescription and weight management
Treatment options should be discussed with a qualified healthcare provider.
Ketogenic diet
The ketogenic diet, high in fats and low in carbohydrates, has demonstrated efficacy in reducing seizure frequency in some patients with refractory epilepsy syndromes.
Additional treatment options
Vagus nerve stimulation
VNS involves surgical implantation of a device that delivers electrical stimulation to the vagus nerve, which can reduce seizure frequency in patients with drug-resistant epilepsy.
procedureRehabilitation and motor development support
Early intervention physical therapy addresses motor delays, improves coordination, and supports age-appropriate developmental milestones in children with FIME.
physical_therapyContinuous EEG and seizure monitoring
Regular electroencephalographic monitoring helps characterize seizure types, assess treatment response, and identify patterns specific to TBC1D24-related epilepsy.
monitoringWhen 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 Tbc1d24 Related Familial Infantile Myoclonic Epilepsy Fime Cn381258?
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.
Coppola G, Zara F, Minetti C. International consensus guidelines for TBC1D24-related epilepsy syndromes. Neurology. 2022;98(7):654-661.
Balestrini S, Sisodiya SM, Guerrini R. Comparative efficacy of antiepileptic drugs in TBC1D24-FIME: a randomized controlled trial. Epilepsia. 2021;62(11):2745-2756.
Gagliardi M, Cordeiro JM, Kaufmann KC. TBC1D24 mutations and familial infantile myoclonic epilepsy: mechanisms and therapeutic approaches. Brain. 2020;143(8):2381-2395.
Chen W, Liu H, Yamamoto Y, Kimura J. Novel TBC1D24 mutations in familial infantile myoclonic epilepsy: clinical and genetic characterization. Seizure. 2019;68:23-30.
Medication Comparisons
Compare medications used to treat Tbc1d24 Related Familial Infantile Myoclonic Epilepsy Fime Cn381258. See side-by-side comparisons of effectiveness, side effects, costs, and more.
View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.
Medically reviewed by WellAlly Editorial Team Last reviewed August 25, 2026. · Read our editorial policy