UNITY screens for the following genetic conditions & antigens
Recessive
Aneuploidy
Fetal Antigens
Cystic fibrosis
Spinal muscular atrophy
Sickle cell disease
Alpha thalassemia
Beta thalassemia
Trisomy 21
Trisomy 13
Trisomy 18
Sex chromosome aneuploidy
D for RhD negative patients
C, c, D, E, Duffy (Fya), or Kell (K) for alloimmunized patients
How is UNITY Screen different from other NIPTs?
Get more information from a maternal blood sample. No paternal sample needed.
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The NIPT that identifies fetal risks beyond chromosome abnormalities
Aneuploidies, recessive conditions, and red blood cell fetal antigens at 10+ weeks.
No partner sample needed.
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UNITY is a screening test. Any high-risk result should be followed up with diagnostic testing.
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Recessive
Cystic fibrosis
Spinal muscular atrophy
Sickle cell disease
Alpha thalassemias
Beta thalassemias
Aneuploidy
Trisomy 21
Trisomy 18
Trisomy 13
Sex chromosome aneuploidy
D for RhD negative patients
C, c, D, E, Duffy (Fya), or Kell (K) for alloimmunized patients
Fetal Antigens