Prévue 預康檢 T21 Premium（由婦產科醫生抽血）
$5,600.00 Original price was: $5,600.00.$3,800.00Current price is: $3,800.00.
專門的血液檢測以篩查影響胎兒發展的異常染色體，採用全基因組測序方法全面覆蓋所有染色體，準確度99.9％。可以在懷孕的第 10 周進行，不會增加您孕期的風險。如檢測結果屬高風險，將會由婦產科醫生講解報告及高達 USD300 高風險患者測試資助*。
Prévue 預康檢 T21 無創性產前檢查 Premium 可檢測 22 項染色體分析 + 性染色體分析 + 116 項微缺失分析 + 胎兒性別分析
*資助只適用於染色體異常結果，並不包括微缺失症候群
如需查詢有關 Prévue 預康檢 T21 無創性產前檢查服務計劃詳情，可以填妥以下表格聯絡我們或 WhatsApp 96601317
Basic 與 Premium 計劃分別
| 康盛T21 BASIC | 康盛T21 PREMIUM | |
|---|---|---|
| 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） | ||
| $3,300 | $3,800 | |
| 查詢 | 查詢 |
116 種微缺失綜合症
| 1p36 deletion syndrome | Currarino syndrome | 16p13.11 deletion syndrome |
| 2q33.1 deletion syndrome | 7q36.3 duplication syndrome | Polycystic kidney disease, infantile severe, with tuberous sclerosis (PKDTS) |
| Wolf-Hirschhorn syndrome | 8p11.2 deletion syndrome | Rubinstein-Taybi syndrome |
| Cri Du Chat syndrome | 8p23.1 deletion syndrome | Alpha-thalassemia/mental retardation syndrome, chromosome 16-related (ATR-16 syndrome) |
| Williams-Beuren syndrome | 8q12 microduplication syndrome | 16q22 deletion syndrome |
| Jacobsen syndrome | Nablus mask-like facial syndrome (NMLFS) | Smith-Magenis syndrome |
| Prader-willi / Angelman syndrome | Trichorhinophalangeal syndrome type 2 (TRPS2) | Yuan-Harel-Lupski syndrome (YUHAL) |
| DiGeorge syndrome | 9p deletion syndrome | 17p12 deletion syndrome |
| 1p32-p31 deletion syndrome | 9p13 microdeletion syndrome | 17p12 duplication syndrome |
| 1q41-q42 deletion syndrome | 9p24.3 deletion syndrome | 17p13.1 deletion syndrome |
| 1q43-q44 deletion syndrome | 9q33.3q34.11 microdeletion syndrome | Miller-Dieker lissencephaly syndrome (MDLS) (loss) |
| 2p12-p11.2 deletion syndrome | Early infantile epileptic encephalopathy 4 (EIEE4) | Miller-Dieker lissencephaly syndrome (MDLS) (gain) |
| 2p15-p16.1 deletion syndrome | Kleefstra syndrome 1 (KLEFS1) | 17p13.3 telomeric duplication syndrome |
| 2q13 deletion syndrome | 10p11.21-p12.31 microdeletion syndrome | 17q12 deletion syndrome |
| 2q13 duplication syndrome | DiGeorge syndrome/velocardiofacial syndrome complex 2 (DSG2) | 17q21.31 deletion syndrome |
| 2q31.1 microdeletion syndrome | 10q22.3-q23.2 deletion syndrome | 17q23.1-q23.2 deletion syndrome |
| 2q31.1 duplication syndrome | Split-hand/foot malformation 3 (SHFM3) | Tetrasomy 18p syndrome |
| 2q35 duplication syndrome | 10q26 deletion syndrome | 18p deletion syndrome |
| 3p25.3 deletion syndrome | Potocki-Shaffer syndrome | 18q deletion syndrome |
| 3pter-p25 deletion syndrome | WAGR syndrome | 19p13 duplication syndrome |
| 3q13.31 deletion syndrome | WAGRO syndrome | 19q13.11 microdeletion syndrome |
| Dandy-Walker syndrome (DWS) | 11q13.2-q13.4 deletion syndrome | 20p13 microdeletion syndrome |
| 3q26 microduplication syndrome | 11q22.2-q22.3 microdeletion syndrome | 21q22.11-q22.12 microdeletion syndrome |
| 3q29 deletion syndrome | 11q23 deletion syndrome | 22q11.2 deletion syndrome (distal, D-E/F) |
| 4q21 deletion syndrome | 12p12.1 microdeletion syndrome | 22q11.2 deletion syndrome (LCR22 B/C-D) |
| Axenfeld-Rieger syndrome, type 1 (RIEG1) | 12q14 microdeletion syndrome | 22q13 deletion syndrome |
| 5p13 duplication syndrome | 12q15q21.1 microdeletion syndrome | 22q13 duplication syndrome |
| 5q12 deletion syndrome | 13q14 deletion syndrome | Xp11.22 duplication syndrome |
| 5q14.3 deletion (proximal) syndrome | 14q11-q22 deletion syndrome | Xp11.22-p11.23 duplication syndrome |
| Sotos syndrome | Frias syndrome | Xp11.23 microdeletion syndrome |
| 6p22 microdeletion syndrome | 14q24.1-q24.3 microdeletion syndrome | Xp11.3 deletion syndrome |
| 6q11-q14 deletion syndrome | 15q13.3 deletion syndrome (BP4 to BP5) (loss) | Xp21 microdeletion syndrome |
| 6q24-q25 deletion syndrome | 15q13.3 deletion syndrome (BP4 to BP5) (gain) | Xp21.2 microduplication syndrome |
| Coffin-Siris syndrome 1 (CSS1) | 15q14 microdeletion syndrome | Xp22.31 microdeletion syndrome |
| Chordoma | 15q25.2 deletion (proximal) syndrome | Xq21 microdeletion syndrome |
| Greig cephalopolysyndactyly syndrome (GCPS) | 15q26-qter deletion syndrome | Xq22.3 telomeric deletion syndrome |
| 7p22.1 microduplication syndrome | 16p11.2-p12.2 microduplication syndrome | Xq27.3-q28 duplication syndrome |
| 7q11.23 deletion (distal) syndrome | 16p12.2 deletion (proximal) syndrome | Xq28 deletion syndrome |
| Williams-Beuren syndrome (WBS) | 16p13.11 duplication syndrome |