MeSH 搜索器

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.
推出的年份: 2002
副标题
树号: C14.280.067.565.720, C14.280.123.625.720, C16.131.240.400.715.720, C23.550.073.547.720
MeSH 单一 ID: D029597
进入的组:
  • 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
早前的内容:
  • Long QT Syndrome (1985-2001)

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