GeneSafe ™ INHERITED – £ 1000

GeneSafe ™ £1000

Genesafe Facilitates Early Diagnosis Of Single-Gene Disorders. The First Non-Invasive Prenatal Test that Screens Multiple Genes For Mutations Causing Severe Genetic Disorders In The Foetus .

GeneSafe works as a complementary screen to traditional and genome-wide NIPT PrenatalSafe KARYO. GeneSafe screens for several life-altering genetic disorders that are not screened with current NIPT technology, allowing for a more complete picture of the risk of a pregnancy being affected by a genetic disorder.

All pregnant women regardless of age are at equal risk of the genetic conditions screened by GeneSafe. Although the occurrence of each disorder is relatively rare, the cumulative rate of these conditions (~1 to 600) is similar to that of Down Syndrome, Edwards syndrome, Patau Syndrome, in younger women.

To Contact us for more information to know about these blood test call  📞 01138301371  to speak with the Healthcare Professional

 

GeneSafe ™ INHERITED – £ 1000

  • This test screens for 5 common inherited recessive genetic disorders, such as Cystic Fibrosis, Beta-Thalassemia, Sickle cell anaemia, Deafness autosomal recessive type 1a and 1b.
  • Allows detection of common inherited disorders within the foetus.
  • Genes screened: CFTR, CX26 (GJB2), CX30 (GJB6), HBB .
  • For further information,Click HERE or the image to download a copy of the brochure.

For further information, please see the test provider’s Technical Analysis Report by  clicking here

To Book this NIPT Test, please Click   BOOK NOW

 

GeneSafe ™ De Novo – £ 1000

This test screens for 44 severe genetic disorders due to de novo mutations (a gene mutation that is not inherited) in 25 genes. 

  • Many disorders screened with GeneSafe De Novo are not typically associated with abnormal prenatal ultrasound findings (especially in the first trimester), or may not be evident until late second/third trimester when confirmatory invasive testing can pose a risk of pre-term birth, or baby’s health after delivery.
  • Genes screened: ASXL1, BRAF, CBL, CHD7, COL1A1, COL1A2 , COL2A1, FGFR2, FGFR3, HDAC8, JAG1, KRAS, MAP2K1, MAP2K2, MECP2, NIPBL, NRAS, NSD1, PTPN11, RAF1, RIT1, SETBP1, SHOC2, SIX3, SOS1
  • For further information,Click HERE or the image to download a copy of the brochure.

For further information, please see the test provider’s Technical Analysis Report by  clicking here

To Book this NIPT Test, please Click   BOOK NOW

 

GeneSafe™ Complete – £ 1500  

This test screens for both inherited and de novo single-gene disorders and represents a combination of the tests GeneSafe Inherited and GeneSafe De Novo providing a complete picture of the pregnancy risk. 

  • GeneSafe Inherited that screens for 5 common inherited recessive genetic disorders, such as Cystic Fibrosis, Beta-Thalassemia, Sickle cell anaemia, Deafness autosomal recessive type 1a and 1b.Allows detection of common inherited disorders within the foetus.Genes screened: CFTR, CX26 (GJB2), CX30 (GJB6), HBB .
  • GeneSafe ™ De Novo that screens for 44 severe genetic disorders due to de novo mutations (a gene mutation that is not inherited) in 25 genes. Many disorders screened with GeneSafe De Novo are not typically associated with abnormal prenatal ultrasound findings (especially in the first trimester), or may not be evident until late second/third trimester when confirmatory invasive testing can pose a risk of pre-term birth, or baby’s health after delivery. Genes screened: ASXL1, BRAF, CBL, CHD7, COL1A1, COL1A2 , COL2A1, FGFR2, FGFR3, HDAC8, JAG1, KRAS, MAP2K1, MAP2K2, MECP2, NIPBL, NRAS, NSD1, PTPN11, RAF1, RIT1, SETBP1, SHOC2, SIX3, SOS1
  • For further information,Click HERE or the image to download a copy of the brochure.

For further information, please see the test provider’s Technical Analysis Report by  clicking here

 

To Book this NIPT Test, please Click   BOOK NOW

 

 

Genetic counselling is available to all PrenatalSAFE clients. Contact us about this service and we will put you in touch with someone who is trained to talk you through your result when there is a Positive Outcomes. 

For further information, please see the test provider’s Technical Analysis Report by clicking here.

Please note

  • We will require details of your GP / Health Care Professional, which may be requested prior to or at the time of the scan.
  • This scan requires access to the area of interest, therefore it is recommended to wear loose clothing to facilitate this process.
  • Blood results require interpretation and All results should be shared with your regular healthcare professional / GP / Fertility specialist.
  • All of our first line ultrasound scans & health Blood tests are optional. You must be at least 16 years old and you should have no existing medical condition or treatment pending that relates to the scan/blood test  you are booking. If you are in any doubt about having any type of test, you should consult your GP.
  • The Geneticist, in the context of Genetic Counselling, will explain in detail the test result and advise to confirm the result by invasive prenatal diagnosis. is provided as part of this Blood test Services. Customers regular Healthcare professional / GP / Fertility specialist is responsible for ensuring appropriate counselling provided to the patient.

 

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