Vistara 胎兒單基因突變檢測

婦健 Femina Healthcare 4D Ultrasound, Prenatal Diagnosis & Treatment Centre 8 704-707 ( A2 )Suite 704-707, Grand Centre, 8, Humphrey Avenue, Tsim Sha Tsui (TST MTR A2 Exit) 23682333

Non-Invasive Prenatal Test for Single Gene Mutation

VISTARA, 30個胎兒單基因突變檢測

Vistara Booking Telephone: 23682333

預訂電話: 23682333

中國大陸客戶: 0085223682333

We strive to ensure you have a healthy baby.

我們努力幫助您生一個健康的BB

Every year in Hong Kong, many healthy parents have abnormal babies.

Why?

Hundreds of baby born with Denovo gene mutations (10/1000).

每年在香港有數百名異常出生的健康父母因香港的新基因突變 (10/1000)。

Monogenic single gene mutation is more common than Down syndrome (10/1000).

https://www.who.int/genomics/public/geneticdiseases/en/

多於唐氏綜合症的發病率 (10/1000)

To ensure having a health baby, one should consider this test.

為了確保有一個健康寶寶,應該考慮這個測試。這些疾病可以導致智障 (新的基因突變)

VISTARA 30 De Novo new gene mutations, tests after 10 weeks

Image result for achondroplasia

Charge 特價: $14,000 (original price 價 $20,000)

These mutation may affect babies heart, bone and brain.

Chance 1 in 600, more than the chance of having a Down Syndrome baby.

Children born with these conditions have severe disabilities.

They need to be care by parent throughout their life.

To ensure having a health baby, one should consider this test.

胎兒基因突變可以影響心臟,骨骼腦和神經系統

這些疾病一些也可以導致智障

發病率每六百人中就有一人,超過唐氏綜合徵的機率 ( 新的基因突變)

大多數受影響的孩子需要父母一生照顧

為了確保有一個健康寶寶,應該考慮這個測試。

Who should have Vistara test? 誰應該接受Vistara檢查?

1. Father more than 45 years old (risk of single mutation is increased)

父親超過45歲(單突變的風險增加)

2. IVF pregnancy (IVF) 受娠

3. Increased nuchal translucency 增加頸部半透明度

4. Ultrasound scan suspicion of one or the following conditions

超聲波掃描懷疑有問題

5. Fetus long bones short 胎儿长骨比正常

6. Radiation exposure during pregnancy 早孕有辐射

Usually perform after 10 weeks pregnant and take 3 weeks to get result

通常在懷孕10週後進行,並需要3週才能獲得結果

VISTARA can detect the following medical conditions:

https://www.natera.com/vistara

Achondroplasia, Osteogenesis Imperfecta, Thanatophoric Dysplasia 1 & 2

Hypochondroplasia & Ehlers Danlos syndrome.

Tuberous sclerosis 1 & 2, Epileptic Encephalopathy

Intellectual disability (SYNGAP1).

Noonan syndrome, Sotos syndrome, Apert syndrome, Rett syndrome

Muenke syndrome, CHARGE syndrome, LEOPARD syndrome

Pfeiffer syndrome, Jackson Weiss syndrome,

Juvenile myelomonocytic leukemia.

可以檢測到以下基因突變 :

軟骨發育不全

成骨不全

比非發育不良

Ehlers Danlos埃勒丹羅斯綜合症

結節性硬化症1和2

癲癇性腦病

智力殘疾(SYNGAP1)

Noonan努南綜合徵

Sotos索托斯綜合徵

Apert開口綜合徵

Rett雷特綜合徵

Muenke綜合徵

CHARGE充電綜合徵

LEOPARD豹綜綜合徵

Pfeiffer綜合徵

Jackson Weiss傑克遜韋斯綜合徵,

少年髓單核細胞白血病。