AUTOGEN PANEL
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Included Tests
Chromosome analysis of cord blood is a genetic test performed on a sample of blood taken from the umbilical cord after birth.This test examines the chromosomes, which are thread - like structures that contain genetic material.Chromosome analysis can help identify chromosomal abnormalities, such as Down syndrome, Turner syndrome, or Klinefelter syndrome.These abnormalities can affect a child physical development, intellectual abilities, and overall health. Cord blood chromosome analysis is often recommended for newborns with birth defects, developmental delays, or other concerning symptoms.
THIS TEST MEASURES THE LEVEL OF IGM ANTIBODIES IN YOUR BLOOD THAT TARGET PHOSPHOLIPIDS, A TYPE OF FAT MOLECULE. THESE ANTIBODIES CAN INTERFERE WITH BLOOD CLOTTING, POTENTIALLY LEADING TO COMPLICATIONS LIKE BLOOD CLOTS, MISCARRIAGES, OR STROKES. HIGH LEVELS OF IGM PHOSPHOLIPID ANTIBODIES MAY INDICATE AN AUTOIMMUNE DISORDER CALLED ANTIPHOSPHOLIPID SYNDROME (APS).
CARDIOLIPIN ANTIBODIES ARE USEFUL IN IDENTIFYING PATIENTS WITH AN INCREASED RISK OF THROMBOSIS, RECURRENT SPONTANEOUS ABORTIONS AND PHOSPHOLIPID ANTIBODY SYNDROME. CARDIOLIPIN ANTIBODY IGG IS THE MOST SENSITIVE BUT THE LEAST SPECIFIC ANTIBODY.
CARDIOLIPIN ANTIBODIES ARE USEFUL IN IDENTIFYING PATIENTS WITH AN INCREASED RISK OF THROMBOSIS, RECURRENT SPONTANEOUS ABORTIONS AND PHOSPHOLIPID ANTIBODY SYNDROME. CARDIOLIPIN ANTIBODY IGM IS LESS SENSITIVE BUT MORE SPECIFIC THAN CARDIOLIPIN ANTIBODY IGG.
TESTING FOR PHOSPHOLIPID ANTIBODIES IS INDICATED IN CASES OF UNEXPLAINED ARTERIAL / VENOUS THROMBOSIS, PREGNANCY WITH UNEXPLAINED FETAL DEATHS, SPONTANEOUS ABORTIONS, PRESENCE OF UNEXPLAINED CUTANEOUS CIRCULATORY DISTURBANCE LIKE LIVIDO RETICULARIS AND PRESENCE OF SYSTEMIC RHEUMATIC DISEASE LIKE LE. THIS TEST IS ALSO USED IN CASES OF UNEXPLAINED THROMBOCYTOPENIA, HEMOLYTIC ANEMIA & NON-BACTERIAL THROMBOTIC ENDOCARDITIS.
The Lupus Anticoagulant by dRVVT (dilute Russell's viper venom time) test is a coagulation assay used to detect the presence of lupus anticoagulants (LA), which are a type of antiphospholipid antibodies. Despite their name, these antibodies are not typically associated with bleeding disorders or systemic lupus erythematosus and are in fact linked to an increased risk of blood clots (thrombosis). The dRVVT test works by using a diluted venom that directly activates Factor X of the coagulation cascade. A prolonged clotting time in the initial screening phase suggests the presence of an inhibitor. This is followed by a confirmatory test using an excess of phospholipids. If the prolonged clotting time corrects (shortens) in the confirmatory step, it indicates that the inhibitor is phospholipid-dependent, which is a characteristic of lupus anticoagulants.
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5 mL (3 mL min.) Whole blood in 2 Green Top (Sodium Heparin) tubes each of Husband & Wife. Ship refrigerated immediately. DO NOT FREEZE. Specimen must reach Lab within 24 hours. Duly filled Chromosome and FISH analysis Requisition form is mandatory AND 3 mL Whole blood in 1 Blue Top (Sodium Citrate) tube. Mix thoroughly by inversion. Transport to Lab within 4 hours. If this is not possible, make PPP within 1 hour of collection as follows: Centrifuge sample at 3600 rpm for 15 min. & transfer supernatant to a clean plastic tube. Centrifuge this supernatant again at 3600 rpm for 15 min. & finally transfer the supernatant (PPP) to 1 labelled clean plastic screw capped vial. FREEZE IMMEDIATELY. Ship frozen. Overnight fasting is preferred. Duly filled AND 4 mL (3 mL min.) Serum from 2 SSTs. Ship refrigerated or frozen. It is recommended that patient discontinues Heparin for 1 day and Oral Anticoagulants for 7 days prior to sampling as these drugs may affect test results. Discontinuation should be with prior consent from the treating Physician.
Culture, Robotic Microscopy, Karyotype; Electromechanical Clot Detection; EIA
Overnight fasting is preferred. It is recommended that patient discontinues Heparin for 1 day and Oral Anticoagulants for 7 days prior to sampling as these drugs may affect test results. Discontinuation should be with prior consent from the treating Physician. .
