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Premature Ovarian Failure Panel

(4 Customer Reviews)
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17-gene panel that includes assessment of noncoding variants. This panel Is ideal for patients with a clinical suspicion of premature ovarian failure.

This test includes the analysis of the CGG repeat region in the 5’-UTR of the FMR1 gene using PCR amplification and fragment size analysis to determine CGG repeat length. 

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Test Features

Genetic factors can play an important role in both male and female infertility. Our Fertility Genetics Panel is designed to identify inherited and chromosomal causes that may affect reproductive health, fertility potential, and family planning decisions.

For women, testing may help identify genetic causes of: ●Premature Ovarian Insufficiency (POI) / Premature Ovarian Failure ●Diminished ovarian reserve ●Recurrent pregnancy loss ●Congenital reproductive tract abnormalities For men, testing may help identify genetic causes of: ●Low sperm count (oligozoospermia) ●Absence of sperm (azoospermia) ●Impaired sperm production ●Chromosomal abnormalities affecting fertility

●Couples experiencing difficulty conceiving ●Individuals with unexplained infertility ●Patients considering IVF or assisted reproduction ●Individuals with recurrent miscarriage ●Men with abnormal semen analysis results ●Women with early menopause or premature ovarian insufficiency

●Identifies underlying genetic causes of infertility ●Supports personalised fertility treatment planning ●Helps guide IVF and reproductive decisions ●Assesses potential risks for future offspring ●Provides valuable information for family planning

Using a blood or saliva sample, our advanced genetic analysis examines genes and chromosomal changes associated with reproductive health and fertility. Results are interpreted by experienced genetics specialists and can be accompanied by genetic counselling where appropriate. Take the next step towards understanding your fertility with insights that can help inform treatment, reproductive choices, and future family planning.