康盛人生無創性產前檢查

在您懷孕的第10周開始,康盛人生無創性產前檢查可讓你通過簡單抽取血液便可有效地檢測到最常見會影響胎兒發展的染色體異常症。這測試對您懷孕過程中的只會產生極低以至零風險。

康盛人生無創性產前檢查
讓您準確瞭解胎兒的健康狀況

美國婦產科醫生學會(ACOG)建議任何年齡孕婦都應做染色體異常篩查,以評估胎兒患有染色體疾病的風險。

染色體異常或相關疾病的風險會隨著孕婦的年齡增加而升高

據統計,大部份誕下患有唐氏綜合症嬰兒的產婦都是35歲以下。這也意味著染色體異常的發病率與婦女年齡無關,任何年齡層的婦女都有可能產下患兒。

更精確的無創性產前檢測
減低入侵性檢測風險

傳統的產前檢測如血清測試,頸皮厚度掃瞄和綜合檢測,假陽性的機率高達5%以上。即是透過這些產前檢測而被診斷為高風險一族的胎兒,實質上只有2-3%是患上唐氏綜合症。而餘下的實際是正常卻被誤診為高危一族。

比起傳統的產前檢測,康盛人生無創性產前檢查擁有較高的準確度,因此選用康盛人生無創性產前檢查可降低入侵性檢查可能引致流產機會。

康盛人生無創性產前檢查優勢

無創性產前檢查服務計劃比較

無創性產前檢查 Basic (單胎適用)

無創性產前檢查 Premium (單胎適用)

胎兒性別(選擇性)
三染色體
T21 唐氏綜合症
T18 愛德華氏綜合症
T13 巴陶氏症
其他三染色體(19項)
性染色體
X 單染色體症(透納氏症)
XXY 性染色體(克氏症候群)
XXX性染色體體(三染色體 X 症候群)
XYY 性染色體症(超雄綜合症)
微缺失症候群
1p36 微缺失分析
2q33.1 微缺失分析
4p16.3 微缺失分析(沃夫 – 賀許宏氏症候群)
5p16.3 微缺失分析(貓哭症候群)
7q11.23 微缺失分析(威廉氏症候群)
11q23 微缺失分析(雅各森症候群)
15q11.2-q13 微缺失分析(普瑞德威利症候群)
22q11.2 微缺失分析(迪喬治症候群)
其他微缺失症候群(108項)

116 種微缺失綜合症

1p36 deletion syndrome
9p24.3 deletion syndrome
Miller-Dieker lissencephaly syndrome (MDLS) (loss)
2q33.1 deletion syndrome
9q33.3q34.11 microdeletion syndrome
Miller-Dieker lissencephaly syndrome (MDLS) (gain)
Wolf-Hirschhorn syndrome
Early infantile epileptic encephalopathy 4 (EIEE4)
17p13.3 telomeric duplication syndrome
Cri Du Chat syndrome
Kleefstra syndrome 1 (KLEFS1)
17q12 deletion syndrome
Williams-Beuren syndrome
10p11.21-p12.31 microdeletion syndrome
17q21.31 deletion syndrome
Jacobsen syndrome
DiGeorge syndrome/velocardiofacial syndrome complex 2 (DSG2)
17q23.1-q23.2 deletion syndrome
Prader-willi / Angelman syndrome
10q22.3-q23.2 deletion syndrome
Tetrasomy 18p syndrome
DiGeorge syndrome
Split-hand/foot malformation 3 (SHFM3)
18p deletion syndrome
1p32-p31 deletion syndrome
10q26 deletion syndrome
18q deletion syndrome
1q41-q42 deletion syndrome
Potocki-Shaffer syndrome
19p13 duplication syndrome
1q43-q44 deletion syndrome
WAGR syndrome
19q13.11 microdeletion syndrome
2p12-p11.2 deletion syndrome
WAGRO syndrome
20p13 microdeletion syndrome
2p15-p16.1 deletion syndrome
11q13.2-q13.4 deletion syndrome
21q22.11-q22.12 microdeletion syndrome
2q13 deletion syndrome
11q22.2-q22.3 microdeletion syndrome
22q11.2 deletion syndrome (distal, D-E/F)
2q13 duplication syndrome
11q23 deletion syndrome
22q11.2 deletion syndrome (LCR22 B/C-D)
2q31.1 microdeletion syndrome
12p12.1 microdeletion syndrome
22q13 deletion syndrome
2q31.1 duplication syndrome
12q14 microdeletion syndrome
22q13 duplication syndrome
2q35 duplication syndrome
12q15q21.1 microdeletion syndrome
Xp11.22 duplication syndrome
3p25.3 deletion syndrome
13q14 deletion syndrome
Xp11.22-p11.23 duplication syndrome
3pter-p25 deletion syndrome
14q11-q22 deletion syndrome
Xp11.23 microdeletion syndrome
3q13.31 deletion syndrome
Frias syndrome
Xp11.3 deletion syndrome
Dandy-Walker syndrome (DWS)
14q24.1-q24.3 microdeletion syndrome
Xp21 microdeletion syndrome
3q26 microduplication syndrome
15q13.3 deletion syndrome (BP4 to BP5) (loss)
Xp21.2 microduplication syndrome
3q29 deletion syndrome
15q13.3 deletion syndrome (BP4 to BP5) (gain)
Xp22.31 microdeletion syndrome
4q21 deletion syndrome
15q14 microdeletion syndrome
Xq21 microdeletion syndrome
Axenfeld-Rieger syndrome, type 1 (RIEG1)
15q25.2 deletion (proximal) syndrome
Xq22.3 telomeric deletion syndrome
5p13 duplication syndrome
15q26-qter deletion syndrome
Xq27.3-q28 duplication syndrome
5q12 deletion syndrome
16p11.2-p12.2 microduplication syndrome
Xq28 deletion syndrome
5q14.3 deletion (proximal) syndrome
16p12.2 deletion (proximal) syndrome
Sotos syndrome
16p13.11 duplication syndrome
6p22 microdeletion syndrome
16p13.11 deletion syndrome
6q11-q14 deletion syndrome
Polycystic kidney disease, infantile severe, with tuberous sclerosis (PKDTS)
6q24-q25 deletion syndrome
Rubinstein-Taybi syndrome
Coffin-Siris syndrome 1 (CSS1)
Alpha-thalassemia/mental retardation syndrome, chromosome 16-related (ATR-16 syndrome)
Chordoma
16q22 deletion syndrome
Greig cephalopolysyndactyly syndrome (GCPS)
Smith-Magenis syndrome
7p22.1 microduplication syndrome
Yuan-Harel-Lupski syndrome (YUHAL)
7q11.23 deletion (distal) syndrome
17p12 deletion syndrome
Williams-Beuren syndrome (WBS)
17p12 duplication syndrome
Currarino syndrome
17p13.1 deletion syndrome
7q36.3 duplication syndrome
8p11.2 deletion syndrome
8p23.1 deletion syndrome
8q12 microduplication syndrome
Nablus mask-like facial syndrome (NMLFS)
Trichorhinophalangeal syndrome type 2 (TRPS2)
9p deletion syndrome
9p13 microdeletion syndrome

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    安康檢代謝病篩查服務Bebegene寶貝基因篩查服務IgE過敏測試服務康盛人生無創性產前檢查(NIPT)隱性遺傳病基因測試其他查詢