【佳學基因檢測】沃德-羅馬諾綜合征基因解碼、基因檢測
基因解碼導讀：
沃德-羅馬諾綜合征是英文Ward-Romano Syndrome的中文翻譯，它又叫沃德-羅馬綜合征，WRS綜合征。是一種常染色體顯形遺傳的長QT綜合征(LQTS)，臨床表現為反反復作的暈厥、抽搐、致命性心律失常(特別是由于心臟復極延長所致先進扭轉型室速)和猝死。佳學基因通過基因解碼技術在發(fā)病前、婚前、孕前分析發(fā)病原因，避免胎兒的再次出生，并為患者提供針病因的治療依據。
什么樣的人應當做沃德-羅馬諾綜合征基因解碼、基因檢測？
患者心臟節(jié)律紊亂，心律失常。這種病癥是一種長QT綜合癥，心臟（心臟）肌肉比正常人花費更長的時間在心跳間重新充電。術語“長QT”是指用心電圖（ECG或EKG）檢測心臟活動時出現的一種心電圖模式。在長QT綜合征的患者中，稱為QT間期的部分心跳異常長。心臟充電所需時間異常導致心律異常。與羅馬 - 沃德綜合征相關的心律失?？蓪е禄柝剩〞炟剩┗蛐呐K驟停和猝死。但是，一些患有羅馬 - 沃德綜合征的人從未遇到任何與該病有關的健康問題。基因解碼根據基因序列明確了15種長QT綜合征。某些類型的長QT綜合征有心臟異?；蚱渌到y(tǒng)問題。羅馬 - 沃德綜合征是指那些只有長QT間期而沒有其他異常的類型。
沃德-羅馬諾綜合征常規(guī)臨床檢查
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臨床表現
根據ECG特征譜、臨床表征和家族史，得出羅馬諾-沃德綜全征的初步診斷.
ECG檢查
Corrected QT (QTc) values on resting ECG. The QTc on resting ECG is neither completely sensitive nor specific for the diagnosis of LQTS. Approximately 25% of individuals with LQTS confirmed by the identification of a pathogenic variant in a LQTS-associated gene may have a normal range QTc (concealed LQTS) [Goldenberg et al 2011]. Also, several other factors can lengthen the QTc interval:
- QT-prolonging drugs
- Hypokalemia
- Certain neurologic conditions including subarachnoid bleed
- Structural heart disease
The following tests are helpful for further evaluation of individuals with "uncertain" QTc values on resting ECG:
- Exercise ECG, which commonly shows failure of the QTc to shorten normally and even prolongation of the QTc interval [Jervell & Lange-Nielsen 1957, Vincent et al 1991, Swan et al 1998, Horner et al 2011, Sy et al 2011]. Many individuals develop characteristic T-wave abnormalities [Zhang et al 2000].
- QTc interval measurement during change from supine to standing position [Viskin et al 2010]
- Intravenous pharmacologic provocation testing (e.g., with epinephrine), which may be helpful by demonstrating inappropriate prolongation of the QTc interval [Ackerman et al 2002]. With the small risk of induction of arrhythmia, such provocative testing is best performed in laboratories experienced in arrhythmia induction and control [Shimizu et al 2004, Vyas et al 2006].
Clinical History
A personal history of syncope, aborted cardiac arrest, or sudden death in a child or young adult may lead to suspicion of LQTS. The syncope is typically precipitous and without warning, thus differing from the common vasovagal and orthostatic forms of syncope in which presyncope and other warning symptoms occur. Absence of aura, incontinence, and postictal findings help differentiate LQTS-associated syncope from seizures.
Family History
A family history of syncope, aborted cardiac arrest, or sudden death in a child or young adult and consistent with autosomal dominant inheritance or autosomal recessive inheritance supports the diagnosis of LQTS.
Establishing the Diagnosis
Schwartz et al [1993] proposed a scoring system to diagnose LQTS on a clinical basis; it was updated by Schwartz & Crotti [2011]. Points are assigned to various criteria (see Table 1).
Table 1.
Scoring System for Clinical Diagnosis of Long QT Syndrome
Findings Points ECG 1 QTc 2 ≥480 ms 3 =460-479 ms 2 =450-459 ms (in males) 1 ≥480 ms during 4th minute of recovery from exercise stress test 1 Torsade de pointes 3 2 T wave alternans 1 Notched T wave in 3 leads 1 Low heart rate for age 4 0.5 Clinical history Syncope 3 With stress 2 Without stress 1 Family history Family member(s) with definite LQTS 5 1 Unexplained sudden cardiac death at age <30 years in immediate family 5 0.5 Total score -
Adapted from Schwartz & Crotti [2011]
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Scoring:
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≤1.0 point = low probability of LQTS
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1.5-3.0 points = intermediate probability of LQTS
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≥3.5 points = high probability of LQTS
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Footnotes:
- 1.
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In the absence of medications or disorders known to affect these electrocardiographic features
- 2.
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QTc (corrected QT) calculated by Bazett's formula where QTc = QT/√RR
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Mutually exclusive
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Resting heart rate <2nd %ile for age
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The same family member cannot be counted for both criteria.
The diagnosis of LQTS is established in a proband with one or more of the following [Priori et al 2013]:
- A risk score of ≥3.5 (see Table 1) in the absence of a secondary cause for QT prolongation
- The presence of a corrected QT interval ≥500 ms in repeated ECGs in the absence of a secondary cause for QT prolongation
- The identification of a pathogenic variant in one of the known to be associated with LQTS (see Tables 2a and 2b)
沃德-羅馬諾綜合征基因解碼
- 致病基因：
根據《人的基因序列變化與人體疾病表征》數據庫，佳學基因發(fā)現和明確了可以引起羅馬諾-沃德綜合征的基因。導致這一疾病發(fā)生的基因有多個，K***1，K***2和S****A基因突變是羅馬 - 沃德綜合征賊常見的致病基因。 這些基因編碼、控制合成人體細胞膜通道。 這些通道蛋白將帶正電荷的離子（如鉀和鈉）輸運進、運出細胞。 在心肌細胞中，這些離子通道蛋白在維持心臟正常節(jié)律方面起著關鍵作用。 基因解碼揭示任何這些基因的突變改變了通道蛋白的結構或功能，影響了離子進入細胞的活動。從而改變心臟的跳動方式，導致羅馬諾 - 沃德綜合征的心律異常。佳學基因解碼提請注意，其他參與離子轉運的基因突變也可以導致羅馬 - 沃德綜合征，基因檢測如果沒能覆蓋這些基因導致致病基因鑒定失敗?；虻膹秃献饔靡彩羌膊“l(fā)生的原因。。
- 遺傳方式：
根據佳學基因《人的基因序列變化與人體疾病表征》數據庫，羅馬諾-沃德綜合征主要按常染色體顯性模式遺傳，但是個性化的發(fā)病原因，會使得不同患者的遺傳模式表現不同。在顯性遺傳中，兩個等位基因中的任何一個發(fā)生突變都會導致患者生病。患者父母往往會有一個患者。但是，子女也可能因為新發(fā)突變而致病，這時發(fā)病原因不是來自父母。使這種情況變得復雜的是，佳學基因發(fā)現這一疾病的外顯率在部分患者會降低。這意味著父母不患病時，子女有可能患病。同樣，父母不患病，在子女中有可能發(fā)生外顯而患病。通過基因解碼明確這些有助于防范。這主要是因為這一疾病的突然來臨，會奪取人的生命。。
沃德-羅馬諾綜合征基因解碼可以區(qū)分：
- 心臟病
- 心肌梗死
- 不同類型的長QT綜合生
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突變基因 不同類型的LQTS 人群占比 A***9 LQTS type 11 Limited A**2 LQTS type 4 <1% C****C LQTS type 8 <1% C**1 LQTS type 14 <1% C***2 LQTS type 15 <1% C**3 LQTS type 9 <1% K***1 LQTS type 5 <1% K***2 LQTS type 6 <1% K***2 LQTS type 7 <1% K***5 LQTS type 13 <1% S***B LQTS type 10 Limited S***1 LQTS type 12 <1%
沃德-羅馬諾綜合征的其他名字
- RWS
- 沃德-羅馬諾綜合征（Ward-Romano Syndrome）
- WRS
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