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
Prévue 預康檢 T21 Basic(由婦產科醫生抽血)
$4,600.00 Original price was: $4,600.00.$3,300.00Current price is: $3,300.00.
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 Basic 可檢測 T21, 18, 13 + 性染色體分析 + 8 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
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 |