Andersen-Tawil syndrome (patient information): Difference between revisions
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==Who is at Highest Risk?== | ==Who is at Highest Risk?== | ||
Patients with ''KCNJ2'' gene, ''KCNJ5'' gene mutations. | |||
==Diagnosis== | ==Diagnosis== | ||
Revision as of 18:58, 17 February 2020
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
Andersen–Tawil syndrome may be classified according to genetic mutations into two groups: Type 1 Andersen–Tawil syndrome and type 2 Andersen–Tawil syndrome.
What are the Symptoms of Andersen–Tawil syndrome?
The most common symptoms of Andersen-Tawil Syndrome include periodic paralysis, ventricular arrhythmias, syncope, muscular weakness, developmental abnormalities, sudden cardiac death and seizures.
What Causes Andersen–Tawil syndrome?
Genes involved in the pathogenesis of Andersen-Tawil syndrome include KCNJ2 gene, KCNJ5 gene and an unknown gene.
Who is at Highest Risk?
Patients with KCNJ2 gene, KCNJ5 gene mutations.
Diagnosis
When to Seek Urgent Medical Care?
Treatment Options
Where to find Medical Care for (Disease name)?
Medical care for (disease name) can be found here.