telangiectasia, hereditary hemorrhagic, type 2

Any hereditary hemorrhagic telangiectasia in which the cause of the disease is a mutation in the ACVRL1 gene.

Also known as: ACVRL1 hereditary hemorrhagic telangiectasia, hereditary hemorrhagic telangiectasia caused by mutation in ACVRL1, telangiectasia, hereditary hemorrhagic, type 2, HHT2, ORW2, Osler Weber Rendu syndrome type 2, hereditary hemorrhagic telangiectasia type 2, telangiectasia hereditary hemorrhagic type 2.

Category: General

Looking into telangiectasia, hereditary hemorrhagic, type 2? See the lab tests healthcare providers may use to investigate telangiectasia, hereditary hemorrhagic, type 2, and learn what each one measures.
Explore tests for telangiectasia, hereditary hemorrhagic, type 2
Symptoms

Symptoms associated with telangiectasia, hereditary hemorrhagic, type 2

The following symptoms have been associated with telangiectasia, hereditary hemorrhagic, type 2 in medical literature. Not everyone experiences the same symptoms.

Tests

Tests used to investigate telangiectasia, hereditary hemorrhagic, type 2

Healthcare providers may order these tests when evaluating telangiectasia, hereditary hemorrhagic, type 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

Urinalysis

Examines urine content to help detect urinary tract infections, kidney disease, and diabetes....

Sample: Urine

Related conditions

Conditions with overlapping symptoms

These conditions share symptoms with telangiectasia, hereditary hemorrhagic, type 2, which is why a clinical evaluation is important.

FAQ

Frequently Asked Questions

What is telangiectasia, hereditary hemorrhagic, type 2?

telangiectasia, hereditary hemorrhagic, type 2 is a health condition described in medical literature. Any hereditary hemorrhagic telangiectasia in which the cause of the disease is a mutation in the ACVRL1 gene.

What are the symptoms of telangiectasia, hereditary hemorrhagic, type 2?

telangiectasia, hereditary hemorrhagic, type 2 is associated with 7 symptoms in the medical literature we index, including Cerebral hemorrhage, Dyspnea, Hematemesis, Hematochezia, Hypertension, Migraine. Symptoms vary widely between individuals.

How is telangiectasia, hereditary hemorrhagic, type 2 diagnosed or investigated?

A healthcare provider may use a combination of medical history, physical examination, and tests. Common tests associated with telangiectasia, hereditary hemorrhagic, type 2 include CBC with Differential, Comprehensive Metabolic Panel (CMP), Urinalysis. 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 telangiectasia, hereditary hemorrhagic, type 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.