Romano-Ward syndrome

Romano-Ward syndrome

Infobox_Disease
Name = Romano-Ward syndrome


Caption = Schematic representation of normal ECG trace "(sinus rhythm)," with waves, segments, and intervals labeled.
DiseasesDB = 11661
ICD10 =
ICD9 = ICD9|794.31
ICDO =
OMIM = 192500
MedlinePlus =
eMedicineSubj =
eMedicineTopic =
MeshID = D029597

Romano-Ward syndrome, is the major variant of long QT syndrome. It is a condition that causes a disruption of the heart's normal rhythm. This disorder is a form of long QT syndrome, which is a heart condition that causes the cardiac muscle to take longer than usual to recharge between beats. If untreated, the irregular heartbeats can lead to fainting, seizures, or sudden death.

Inheritance

Romano-Ward syndrome is inherited in an autosomal dominant pattern. It is the most common form of inherited long QT syndrome, affecting an estimated 1 in 5,000 people worldwide, although more people may be affected but never experience any signs or symptoms of the condition.

Causes

Mutations in the "ANK2, KCNE1, KCNE2, KCNH2, KCNQ1", and "SCN5A" genes cause Romano-Ward syndrome. The proteins made by most of these genes form channels that transport positively-charged ions, such as potassium and sodium, in and out of cells. In cardiac muscle, these ion channels play critical roles in maintaining the heart's normal rhythm. Mutations in any of these genes alter the structure or function of channels, which changes the flow of ions between cells. A disruption in ion transport alters the way the heart beats, leading to the abnormal heart rhythm characteristic of Romano-Ward syndrome.

Unlike most genes related to Romano-Ward syndrome, the "ANK2" gene does not produce an ion channel. The protein made by the "ANK2" gene ensures that other proteins, particularly ion channels, are inserted into the cell membrane appropriately. A mutation in the ANK2 gene likely alters the flow of ions between cells in the heart, which disrupts the heart's normal rhythm and results in the features of Romano-Ward syndrome.

"This article incorporates public domain text from [http://ghr.nlm.nih.gov The U.S. National Library of Medicine] "

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Look at other dictionaries:

  • Romano-Ward syndrome — Romano Ward syndrome. См. синдром Романо Уорда. (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд во ВНИРО, 1995 г.) …   Молекулярная биология и генетика. Толковый словарь.

  • Romano-Ward syndrome — Ro·mano Ward syndrome (ro mahґno wordґ) [C. Romano, Italian physician, born 1923; O.C. Ward, Irish physician, 20th century] see under syndrome …   Medical dictionary

  • Romano-Ward syndrome — the more common, autosomal dominant form of the long QT syndrome, characterized by syncope and sometimes ventricular fibrillation and sudden death …   Medical dictionary

  • Syndrome de romano-ward — Pour les articles homonymes, voir Romano et Ward. Syndrome de Romano Ward …   Wikipédia en Français

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  • Romano-Ward-Syndrom — Dieser Artikel erläutert das Long QT Syndrom; es existiert aber auch das (wesentlich seltenere) Short QT Syndrom. Klassifikation nach ICD 10 I45.8 Sonstige näher bezeichnete kardiale …   Deutsch Wikipedia

  • Ward-Romano syndrome — Ward Ro·ma·no syndrome (wordґ ro mahґno) [Owen Conor Ward, Irish pediatrician, born 1923; Cesarino Romano, Italian pediatrician, born 1924] Romano Ward syndrome …   Medical dictionary

  • Syndrome du qt long — |Le syndrome du QT long est un syndrome phénotypiquement et génétiquement hétérogène qui se caractérise par un allongement de l espace QT sur l électrocardiogramme de surface associé à un risque élevé de torsades de pointe ou de fibrillation… …   Wikipédia en Français

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  • Ward — Cette page d’homonymie répertorie les différents sujets et articles partageant un même nom. Sur les autres projets Wikimedia : « Ward », sur le Wiktionnaire (dictionnaire universel) Ward peut désigner : Sommaire …   Wikipédia en Français

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