What is GeneSAFE™ ?
GeneSafe™ is the first non-invasive prenatal test that screens for both de novo and inherited single-gene disorders in the fetus. Starting from the 10th week of pregnancy, a sample safely taken from the mother’s blood allows for the screening of many hereditary single-gene disorders in the fetus.
Among the currently available PrenatalSafe non-invasive prenatal tests (NIPT), only PrenatalSafe Complete Plus / PrennatalSafe Complete includes the GeneSafe Complete test.
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5 Recessive Disease Screening
- CYSTIC FIBROSIS; GEN CFTR
- AUTOSOMAL RECESSIVE HEARING LOSS- TYPE1A; GEN CX26 (GJB2)
- AUTOSOMAL RECESSIVE HEARING LOSS- TYPE1B; GEN CX30 (GJB6)
- BETA thalassemia; GENE HBB
- SICKLE CELL ANEMIA; GENE HBB
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GeneSafe™ Complete = GeneSafe™ De Novo + GeneSafe™ Inherited
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* GeneSafe de novo inherited single-gene disorders list