DR B Clinic 診所

DR B Clinic 診所 Contact information, map and directions, contact form, opening hours, services, ratings, photos, videos and announcements from DR B Clinic 診所, Doctor, NO 216-217 GROUND FLOOR Jalan SETIA RAJA TAMAN STUTONG INDAH, Kuching.

MEDICAL CLINIC
We provide blood test screening / Vaccination / Wound dressing / General disease treatment / Ultrasound scanning / Antenatal scan / Pap smear / DNA test /NICC / GUT test/ Aesthetic and skin wellness /Functional & Integrative Medicine

29/10/2025

INFLUENZA VACCINE IS NOW AVAILABLE IN OUR CLINIC
(Only Accept WALK IN)
No Pre-Booking

Casual Monday but virus is spreading vigorously , please do your part to wear mask or take care of personal hygiene if y...
20/10/2025

Casual Monday but virus is spreading vigorously , please do your part to wear mask or take care of personal hygiene if you are having common cold symptoms and to avoid from the crowds .

so not all cough and fever has to be on antibiotics, virus is spreading all over the corner, please wear mask and take c...
18/10/2025

so not all cough and fever has to be on antibiotics, virus is spreading all over the corner, please wear mask and take care of personal hygiene

We are excited to announced that we offered GENETIC CARRIER CHECK services for couples plan for future family planning ...
01/08/2025

We are excited to announced that we offered GENETIC CARRIER CHECK services for couples plan for future family planning !

Genetic Carrier screening is a genetic test that helps identify whether a person carries a gene mutation associated with certain autosomal recessive or X-linked genetic disorders. Even if a carrier doesn’t have symptoms of the condition, they can pass the mutation to their children.

Purpose:
Assesses the risk of a couple having a child with a genetic disorder.
Helps in family planning and reproductive decision-making.

When Is It Done?

Before pregnancy (preconception): Allows couples to understand risks and explore options like IVF with preimplantation genetic testing (PGT).

During pregnancy: If not done earlier, it can still provide information about risks and prenatal testing options (e.g., amniocentesis, CVS).

How It Works:

Typically done via blood test or saliva sample.

Screens for mutations in genes linked to conditions up to 900 conditions example :

Cystic Fibrosis (CF)

Spinal Muscular Atrophy (SMA)

Tay-Sachs Disease

Sickle Cell Disease

Fragile X Syndrome (X-linked)

Who Should Consider It?
All couples planning a pregnancy (even without family history, as many carriers have no symptoms).

People with a family history of genetic disorders.

Possible Outcomes & Next Steps:

If only one parent is a carrier: The child is unlikely to have the disorder but may be a carrier.

If both parents are carriers for the same condition: There’s a 25% chance per pregnancy of having an affected child.

Address

NO 216-217 GROUND FLOOR Jalan SETIA RAJA TAMAN STUTONG INDAH
Kuching
93350

Opening Hours

Monday 08:00 - 17:00
Tuesday 08:00 - 17:00
Wednesday 12:00 - 17:00
Thursday 08:00 - 12:00
Friday 08:00 - 17:00
Saturday 08:00 - 17:00

Telephone

+60198575188

Website

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