Genetic carrier screening for family planning

Genetic diseases, or conditions resulting from abnormal inheritance of genetic traits from parents to offspring, often manifest without noticeable symptoms in the parents due to the carriers’ status of abnormal genetic material. However, these abnormal genetic traits can be passed on to future generations, potentially leading to various diseases. Screening for genetic disorders can be invaluable for family planning.

Our Genetic Screening Package utilizes advanced whole exome sequencing technology to analyze genetic information, covering up to 145 commonly identified genetic diseases. These include conditions such as Thalassemia, Fragile X syndrome, Spinal Muscular Atrophy, and Hearing Loss.

Instructions

1. Customers are advised to contact our staff prior to the service.
2. The specimen collection takes 15-30 minutes, and results are expected to be delivery within 45- 60 days.
3. For additional information or appointment rescheduling, please contact us at 02-106-6999 ext. 129 or 269.

Our Genetic Screening Package offers advanced whole exome sequencing to detect up to 145 genetic disorders, including Thalassemia, Fragile X syndrome, and Spinal Muscular Atrophy. Specimen collection takes 15-30 minutes, with results in 45-60 days. Contact us for more info or to reschedule appointments.