Matchmygenome

Service Description

Matchmygenome is a comprehensive Couple Carrier Screen ideal for preconception screening, to determine the carrier status of common genetic disorders in the couple to estimate the risk of passing on a genetic disorder to their future offspring. The high-resolution screening for genetic variants by NGS is recommended as a first-tier genetic test to screen for suspected pathogenic variants. CLINICAL UTILITY -To diagnose carrier status for autosomal & recessive genetic disorders -Differentiation between de novo(new unexplained mutations) and familial history of disorders -To clarify the clinical significance of copy number changes -To influence the management of the conditions/disorders in a better way including lifestyle interventions. WHEN IS THE TEST RECOMMENDED? -Individuals or couples before pregnancy (preconception carrier screening) -A consanguineous couple or couple belonging to the same community or same ethnic group. -Couple has a child suffering from a Mendelian disorder and who are planning to have another child. -Couple with history of miscarriages, recurrent pregnancy loss, infertility, hereditary syndromes -Couple with a family history of a particular recessive disease or a Mendelian disorders -Couple and relatives of identified carriers, or to the partners of people with the disease. Sample Type: Blood in EDTA (from both parents) TAT: 4-6 weeks

Cancellation Policy

For cancellation & refund: Please email us at admin@hassanhealth.com least 1 hour prior to your appointment. If credit card payment has been made, please allow up to 30 working days for refund. *All Prices exclude 14% VAT

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