Romano-Ward Syndrome
A form of long QT syndrome that is without congenital deafness. It is caused by mutation of the KCNQ1 gene which encodes a protein in the VOLTAGE-GATED POTASSIUM CHANNEL.
Year introduced: 2002
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Subheadings:
Tree Number(s): C14.280.067.565.720, C14.280.123.625.720, C16.131.240.400.715.720, C23.550.073.547.720
MeSH Unique ID: D029597
Entry Terms:
- Romano Ward Syndrome
- Syndrome, Romano-Ward
- Ventricular Fibrillation with Prolonged QT Interval
- Long QT Syndrome Type 1
- Long QT Syndrome 1
- Ward-Romano Syndrome
- Syndrome, Ward-Romano
- Ward Romano Syndrome
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