Sickle Cell Anemia Mutation Type

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SickleFREE

 Sickle Cell Disease Screening made Easy!

Sickle cell disease is a group of disorders that affects hemoglobin. People with this disorder have an abnormal hemoglobin called hemoglobin S. It leads to low number of red blood cells (anemia), repeated infections, and periodic episodes of pain. It is inherited in autosomal recessive manner.

SickleFREE is a revolutionary product to screen and detect normal, Sickle cell, carrier and HbSCdisease in 4 EASY STEPS. SickleFREE reduces time and cost with minimal requirements to treat masses across the globe.

Sickle Cell Anemia Mutation Type
Karyotyping - AF/ CVS
Sickle Cell Anemia Mutation Type
Karyotyping - Cord Blood/ Peripheral Venous Blood
Sickle Cell Anemia Mutation Type
PND Karyotyping with QF-PCR
Sickle Cell Anemia Mutation Type
Couple Karyotyping
Sickle Cell Anemia Mutation Type
High Resolution Karyotyping

Comparison

 

FEATURES Double Marker Test Triple Marker Test Quadruple Marker Test
Ideal Period for screening 11th to 13th week of pregnancy 15th to 20th week of pregnancy. 15th to 20th week of pregnancy.
Parameters Beta HCG, PAPP-A Beta HCG, AFP, Unconjugated Estriol Beta HCG, AFP, Unconjugated Estriol, Inhibin-A
Screens For Trisomy - 21 and Trisomy - 18 Trisomy - 21, Trisomy - 18 and Open Neural Tube Defects Trisomy - 21, Trisomy - 18 and Open Neural Tube Defects

 

Sickle Cell Anemia Mutation Type

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Sickle Cell Anemia Mutation Type
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Sickle Cell Anemia Mutation Type

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Sickle Cell Anemia Mutation Type

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Sickle Cell Anemia Mutation Type

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Sickle Cell Anemia Mutation Type

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Sickle Cell Anemia Mutation Type

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