Reproductive Health

Identifying genetic causes of infertility facilitates informed decisions and family planning for your patients. With 10% of infertility cases being linked to genetic factors, their detection can provide vital answers. Genetic testing can be the key for a significant number of infertile couples trying to have children, as understanding the reason for infertility can often lead to success with a range of assisted reproductive techniques.

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CentoScreen® Solo

CentoScreen® is our comprehensive screening panel that covers more than 300 common autosomal recessive and X-linked disorders. It provides the opportunity to make informed decisions and review the range of options available to guide pregnancy and family planning. Includes complete panel evaluation with CNV analysis* of 34 genes.

No. of genes: 330
TAT: 25 days
Coverage: ≥99.00% ≥20x
Details:
NGS including CNV analysis
Sanger sequencing: CYP21A2
Repeat expansion analysis: FMR1
MLPA: SMN1

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CentoScreen® Duo

Includes complete panel evaluation with CNV analysis of 34 genes for each partner.

No. of genes: 330
TAT: 25 days
Coverage: ≥99.00% ≥20x
Details:
NGS including CNV analysis
MLPA: SMN1
Sanger sequencing: CYP21A2
Repeat expansion analysis: FMR1

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CentoScreen® Paired

Includes complete panel evaluation with CNV analysis of 34 genes + risk gene analysis of partners.

No. of genes: 330
TAT: 30 days
Coverage: ≥99.00% ≥20x
Details:
NGS including CNV analysis
Repeat expansion analysis: FMR1
Sanger sequencing: CYP21A2
MLPA: SMN1

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COMMON SYNDROMES AND DISORDERS COVERED
  • Alport disease
  • Bardet-Biedl syndromes
  • Congenital adrenal hyperplasia
  • Cystic fibrosis
  • Fragile X syndrome
  • Glycine encephalopathy
  • Maple syrup urine disease
  • Mucolipidosis, several types
  • Mucopolysaccharidosis, several types
  • Niemann-Pick disease
  • Spinal muscular atrophy
  • Organic acidemias
  • Wilson disease

Infertility panel

Our infertility panel is recommended for patients trying to conceive for one year or longer, with known fertility problems, who have experienced more than one miscarriage, with irregular or absent menstruation, with low sperm count, form, or movement, or with absence of development of secondary sexual features. Our panel includes the most important genes related to infertility in males and females. Knowing the exact cause of infertility allows for better diagnostic decisions and enables enhanced counseling for couples.

No. of genes: 276
TAT: 25 days
Coverage: ≥99.00% ≥20x
Details:
NGS including CNV analysis
Sanger sequencing: CFTR
Repeat expansion analysis: AR, FMR1

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