migraine, familial hemiplegic, 2

Any familial or sporadic hemiplegic migraine in which the cause of the disease is a mutation in the ATP1A2 gene.

Also known as: ATP1A2 familial or sporadic hemiplegic migraine, familial or sporadic hemiplegic migraine caused by mutation in ATP1A2, migraine, familial hemiplegic, 2, migraine, familial hemiplegic, type 2, FHM2, familial hemiplegic migraine type 2, hemiplegic migraine, familial type 2.

Category: General

Looking into migraine, familial hemiplegic, 2? See the lab tests healthcare providers may use to investigate migraine, familial hemiplegic, 2, and learn what each one measures.
Explore tests for migraine, familial hemiplegic, 2
Symptoms

Symptoms associated with migraine, familial hemiplegic, 2

The following symptoms have been associated with migraine, familial hemiplegic, 2 in medical literature. Not everyone experiences the same symptoms.

Tests

Tests used to investigate migraine, familial hemiplegic, 2

Healthcare providers may order these tests when evaluating migraine, familial hemiplegic, 2. 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...

Sample: Blood

Comprehensive Metabolic Panel (CMP)

Measures 14 substances in the blood to assess kidney and liver function, electrolyte balance, and blood sugar ...

Sample: Blood

Related conditions

Conditions with overlapping symptoms

These conditions share symptoms with migraine, familial hemiplegic, 2, which is why a clinical evaluation is important.

FAQ

Frequently Asked Questions

What is migraine, familial hemiplegic, 2?

migraine, familial hemiplegic, 2 is a health condition described in medical literature. Any familial or sporadic hemiplegic migraine in which the cause of the disease is a mutation in the ATP1A2 gene.

What are the symptoms of migraine, familial hemiplegic, 2?

migraine, familial hemiplegic, 2 is associated with 13 symptoms in the medical literature we index, including Bilateral tonic-clonic seizure, Blurred vision, Cerebral edema, Confusion, Diplopia, Drowsiness. Symptoms vary widely between individuals.

How is migraine, familial hemiplegic, 2 diagnosed or investigated?

A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with migraine, familial hemiplegic, 2 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 migraine, familial hemiplegic, 2, please discuss your symptoms with a qualified healthcare provider.

Educational content only: The information on Symptom Database.com is for educational purposes and is not medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider. Read our full disclaimer.