Familial infantile myoclonic epilepsy
Familial infantile myoclonic epilepsy is a medical condition that may be associated with various symptoms and signs.
Category: General
Symptoms associated with Familial infantile myoclonic epilepsy
The following symptoms have been associated with Familial infantile myoclonic epilepsy in medical literature. Not everyone experiences the same symptoms.
Bilateral tonic-clonic seizure
A bilateral tonic-clonic seizure is a seizure defined by a tonic (bilateral increased tone, lasting seconds to...
Blepharospasm
A focal dystonia that affects the muscles of the eyelids and brow, associated with involuntary recurrent spasm...
Focal-onset seizure
A focal-onset seizure is a type of seizure originating within networks limited to one hemisphere. They may be ...
Generalised tonic-clonic seizure without focal onset
A bilateral tonic-clonic seizure with generalized onset is a type of bilateral tonic-clonic seizure characteri...
Generalized myoclonic seizure
A generalized myoclonic seizure is a type of generalized motor seizure characterized by bilateral, sudden, bri...
Seizure
A seizure is an intermittent abnormality of nervous system physiology characterized by a transient occurrence ...
Simple febrile seizure
A short generalized seizure, of a duration of <15 min, not recurring within 24 h, occurring during a febrile e...
Tests used to investigate Familial infantile myoclonic epilepsy
Healthcare providers may order these tests when evaluating Familial infantile myoclonic epilepsy. Test selection is a clinical decision made by a qualified professional.
CBC with Differential
Measures red blood cells, white blood cells, and platelets to help evaluate overall health and detect disorder...
Comprehensive Metabolic Panel (CMP)
Measures 14 substances in the blood to assess kidney and liver function, electrolyte balance, and blood sugar ...
Conditions with overlapping symptoms
These conditions share symptoms with Familial infantile myoclonic epilepsy, which is why a clinical evaluation is important.
Early infantile developmental and epileptic encephalopathy
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Lafora disease
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Self-limited infantile epilepsy
Self-limited infantile epilepsy is a medical condition that may be associated with various symptoms and signs....
Stolerman neurodevelopmental syndrome
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branched-chain keto acid dehydrogenase kinase deficiency
A rare disorder of branched-chain amino acid metabolism characterized by childhood-onset epilepsy, autism and ...
congenital disorder of glycosylation, type IIcc
congenital disorder of glycosylation, type IIcc is a medical condition that may be associated with various sym...
Frequently Asked Questions
What is Familial infantile myoclonic epilepsy?
Familial infantile myoclonic epilepsy is a health condition described in medical literature. Familial infantile myoclonic epilepsy is a medical condition that may be associated with various symptoms and signs.
What are the symptoms of Familial infantile myoclonic epilepsy?
Familial infantile myoclonic epilepsy is associated with 7 symptoms in the medical literature we index, including Bilateral tonic-clonic seizure, Blepharospasm, Focal-onset seizure, Generalised tonic-clonic seizure without focal onset, Generalized myoclonic seizure, Seizure. Symptoms vary widely between individuals.
How is Familial infantile myoclonic epilepsy diagnosed or investigated?
A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with Familial infantile myoclonic epilepsy include CBC with Differential, Comprehensive Metabolic Panel (CMP). This information is educational, not a diagnosis.
Is SymptomDatabase.com diagnosing me?
No. SymptomDatabase.com does not provide diagnosis. If you are concerned you may have Familial infantile myoclonic epilepsy, please discuss your symptoms with a qualified healthcare provider.