Chlamydia trachomatis RNA, TMA, Urogenital
*Build Your Own Panel Eligible [?]
|
$49
|
|
|
Description:
C. trachomatis infections are the leading cause of sexually transmitted diseases in the united states. C. trachomatis is known to cause cervicitis, pelvic inflammatory disease (PID), epididymitis and proctitis. It is also the most frequent cause of non-gonococcal urethritis in men. Among women, the consequences of chlamydial infections are severe if left untreated. Approximately half of chlamydial infections are asymptomatic.
Categories:
Price:
$49
|
|
Chlamydia trachomatis, TMA (Alternate Target), Rectal
*Build Your Own Panel Eligible [?]
|
$347
|
|
|
Description:
Chlamydia trachomatis may infect the anal/rectal canal of sexually active individuals. Detection of this organism may be important for determining the risk for disease progression or transmission.
Categories:
Price:
$347
|
|
Chlamydia trachomatis, TMA (Alternate Target), Urogenital
*Build Your Own Panel Eligible [?]
|
$49
|
|
|
Description:
Several methods are available for the detection of C. trachomatis in clinical specimens, including giemsa staining of tissue, fluorescent antibody staining, culture, and nucleic acid detection. Although culture is very specific, it lacks sensitivity, so recommendations have been put forth to include multiple tests in assisting with a diagnosis of infection, including tests such as the CT/NG Aptima TMA Assay.
Categories:
Price:
$49
|
|
Chlamydophila pneumoniae Antibodies (IgG, IgA, IgM)
*Build Your Own Panel Eligible [?]
|
$344
|
|
|
Description:
Chlamydophila pneumoniae is a common cause of infantile and community-acquired pneumonia.
Categories:
Price:
$344
|
|
Chlamydophila pneumoniae Antibody (IgM)
*Build Your Own Panel Eligible [?]
|
$355
|
|
|
Description:
Chlamydophila pneumoniae is a common cause of infantile and community-acquired pneumonia.
Categories:
Price:
$355
|
|
Chlamydophila pneumoniae, DNA, Qualitative, Real-Time PCR
*Build Your Own Panel Eligible [?]
|
$308
|
|
|
Description:
This test is used to determine the presence of Chlamydophila pneumoniae in a patient's specimen. Organisms may be detected by PCR prior to detection by immunological methods. PCR provides more rapid results than other methods, including culture.
Categories:
Price:
$308
|
|
Chlamydophila psittaci Antibodies (IgG, IgA, IgM)
*Build Your Own Panel Eligible [?]
|
$335
|
|
|
Description:
Psittacosis, also known as parrot's disease, is transmitted to humans from parrots and other birds. Psittacosis is associated with mild illness to severe pneumonia.
Categories:
Price:
$335
|
|
Chlordiazepoxide and Metabolites
*Build Your Own Panel Eligible [?]
|
$325
|
|
|
Description:
This definitive drug assay is used to measure concentrations of chlordiazepoxide, norchlordiazepoxide, and nordiazepam in serum. This therapeutic drug monitoring assay may be used to assess if chlordiazepoxide and metabolites are within therapeutic range. Urine and oral fluid are the specimens of choice for routine monitoring of patients taking prescription drugs.Chlordiazepoxide is a long-acting benzodiazepine used to treat adults for anxiety disorder, preoperative apprehension and anxiety, and withdrawal symptoms of acute alcohol use disorder. It is also used to treat children older than 6 years for anxiety.Chlordiazepoxide has several active metabolites, and prolonged duration of action may lead to serious adverse effects in older individuals, children, and individuals with disabilities or hepatic or renal impairment. Common adverse effects include drowsiness, fatigue, dizziness, ataxia, forgetfulness, slurred speech, irritability, and rash. Chlordiazepoxide intoxication and overdose can be life-threatening, especially when chlordiazepoxide is combined with alcohol and other central nervous system depressants [1,2]. However, routine quantitative tests of chlordiazepoxide are not needed unless medical conditions warrant monitoring or for individuals taking other drugs that increase the risk of intoxication [2].The results of this test should be interpreted in the context of pertinent clinical history and physical examination findings.References1. Chlordiazepoxide. In: Fuller MA, et al, eds. Drug Information Handbook for Psychiatry. 7th ed. Lexi-Comp Inc; 2009:316-319.2. Whyte IM. Benzodiazepines. In: Dart RC, et al. Medical Toxicology. 3rd ed. Lippincott Williams & Wilkins; 2004:811-823.
Categories:
Price:
$325
|
|
Chloride
*Build Your Own Panel Eligible [?]
|
$39
|
|
|
Description:
The Chloride Test is a blood test used to measure the level of chloride, an important electrolyte. Serum chloride is the major extracellular anion and counter-balances the major cation, sodium, maintaining electrical neutrality of the body fluids. Two thirds of the total anion concentration in extracellular fluids is chloride and it is significantly involved in maintaining proper hydration and osmotic pressure. Movement of chloride ions across the red blood cell membrane is essential for the transport of biocarbonate ions in response to changing concentrations of carbon dioxide. Chloride measurements are used in the diagnosis and treatment of electrolyte and metabolic disorders such as cystic fibrosis and diabetic acidosis.
Significant deviations from the normal range may require further evaluation by your physician.
Includes:
Chloride
****Chloride, serum is included in the Comprehensive Metabolic Profile (CMP), Electrolyte Panel and in the Kidney Function Profile.***
Categories:
Blood and blood diseases,
General wellness,
Heart & cholesterol,
Price:
$39
|
|
Chloride, 24-Hour Urine with Creatinine
*Build Your Own Panel Eligible [?]
|
$212
|
|
|
Description:
Urine chloride excretion approximates the dietary intake. The chloride content of most foods parallels that of sodium. An increase in urine chloride may result from water deficient dehydration, diabetic acidosis, Addison's Disease, and salt-losing renal disease. Decreased urine levels are seen in congestive heart failure, severe diaphoresis and in hypochloremic metabolic alkalosis due to prolonged vomiting.
Categories:
Price:
$212
|
|
Chloride, 24-Hour Urine without Creatinine
*Build Your Own Panel Eligible [?]
|
$202
|
|
|
Description:
Urine chloride excretion approximates the dietary intake. The chloride content of most foods parallels that of sodium. An increase in urine chloride may result from water deficient dehydration, diabetic acidosis, Addison's Disease, and salt-losing renal disease. Decreased urine levels are seen in congestive heart failure, severe diaphoresis and in hypochloremic metabolic alkalosis due to prolonged vomiting.
Categories:
Price:
$202
|
|
Chloride, Feces
*Build Your Own Panel Eligible [?]
|
$263
|
|
|
Description:
Measurements of chloride in conjunction with other electrolytes in liquid stool may help differentiate between secretory and osmotic diarrhea. This test may also aid in the diagnosis of primary or secondary chloridorrhea. Diarrhea can be categorized as secretory or osmotic depending on how the water content of stool is drawn in the intestine lumen. Secretory diarrhea is caused by defective electrolyte absorption that increases the stool's electrolyte levels. Conditions associated with secretory diarrhea include infection, neuroendocrine tumors, intestinal resection, diffuse mucosal disease, and congenital chloridorrhea [1]. Congenital chloridorrhea is a rare autosomal-recessive disorder characterized by watery stool containing excessive chloride. Stool chloride levels during perinatal period and infancy are often greater than 120 mmol/L [2]. Similar to congenital chloridorrhea, acquired chloridorrhea may manifest as hypochloremia, metabolic alkalosis, and no chloride in the urine, but the magnitude of excess chloride excretion in the stool is usually less [3]. Low levels of stool chloride may be seen in sodium sulfate-induced diarrhea [4].The results of this test should be interpreted in the context of pertinent clinical and family history and physical examination findings.References1. Schiller LR. Pract Res Clin Gastroenterol. 2012;26(5):551-562.2. Konishi KI, et al. J Pediatr. 2019;214:151-157.e6.3. Kaplan BS, et al. J Pediatr. 1981;99(2):211-214.4. Eherer AJ, et al. Gastroenterology. 1992;103(2):545-551.
Categories:
Price:
$263
|
|
Chloride, Random Urine with Creatinine
*Build Your Own Panel Eligible [?]
|
$212
|
|
|
Description:
Urine chloride excretion approximates the dietary intake. The chloride content of most foods parallel that of sodium. An increase in urine chloride may result from water deficient dehydration, diabetic acidosis, Addison's Disease, and salt-losing renal disease. Decreased urine levels are seen in congestive heart failure, severe diaphoresis and in hypochloremic metabolic alkalosis due to prolonged vomiting.
Categories:
Price:
$212
|
|
Chloride, Random Urine without Creatinine
*Build Your Own Panel Eligible [?]
|
$202
|
|
|
Description:
Urine chloride excretion approximates the dietary intake. The chloride content of most foods parallel that of sodium. An increase in urine chloride may result from water deficient dehydration, diabetic acidosis, Addison's disease, and salt-losing renal disease. Decreased urine levels are seen in congestive heart failure, severe diaphoresis and in hypochloremic metabolic alkalosis due to prolonged vomiting.
Categories:
Price:
$202
|
|
Chlorpromazine
*Build Your Own Panel Eligible [?]
|
$340
|
|
|
Description:
Chlorpromazine is a phenothiazine for treating psychosis and Tourett's syndrome. Monitoring it's level is important to optimize therapy, to avoid toxicity, and to assure compliance.
Categories:
Price:
$340
|
|
Chocolate/Cacao IgG4
*Build Your Own Panel Eligible [?]
|
$254
|
|
Description:
- Detect chocolate related digestive symptoms
- Screen for hidden food sensitivity triggers
- Track skin and energy reactions
Categories:
Price:
$254
|
|
Cholesterol and HDL Cholesterol with Ratio
*Build Your Own Panel Eligible [?]
|
$49
|
|
|
Description:
This panel measures serum concentrations of total cholesterol and high-density lipoprotein (HDL) cholesterol and provides a calculated total cholesterol/HDL cholesterol ratio. Measurements of cholesterol in conjunction with lipoproteins are used primarily in the risk assessment of atherosclerotic cardiovascular disease (ASCVD) [1].Elevated total cholesterol is an established risk factor for atherosclerotic coronary disease [1]. HDL cholesterol level has been inversely related to the ASCVD risk, whereas very high HDL levels may increase all-cause mortality [2]. The cholesterol/HDL cholesterol ratio, also known as atherogenic or Castelli index, has been proposed as a stronger predictor of ASCVD risk than total cholesterol or HDL cholesterol alone [3].Treatment with N-acetyl cysteine for acetaminophen overdose may generate a falsely low result for cholesterol [4]. Venipuncture immediately after or during administration of the painkiller metamizole (dipyrone) may also lead to falsely low results for cholesterol [5].Note: Any or all individual tests from a panel can be ordered separately.The results of this test should be interpreted in the context of pertinent clinical and family history as well as physical examination findings.References1. Meeusen J, et al. Lipids and lipoproteins. In: Rifai R, et al. eds. Tietz Textbook of Laboratory Medicine. 7th ed. Elsevier Inc; 2022.2. Madsen CM, et al. Eur Heart J. 2017;38(32):2478-2486.3. Millan J, et al. Vasc Health Risk Manag. 2009;5:757-765.4. Beckman Coulter AU analyzers. Instructions for use. Beckman Coulter Inc; 2015. Accessed January 19, 2023. https://www.beckmancoulter.com/wsrportal/techdocs?docname=/cis/BAOSR6X16/%25%25/EN_CHOL%20OSR%20General%20Chemistry.pdf5. Gascon N, et al. Clin Chem. 1993;39(6):1033-1036.
Categories:
Price:
$49
|
|
Cholesterol, Total
*Build Your Own Panel Eligible [?]
|
$49
|
|
|
Description:
Total LDL and HDL cholesterol, in conjunction with a triglyceride determination, provide valuable information for the risk of coronary artery disease. Total serum cholesterol analysis is useful in the diagnosis of hyperlipoproteinemia, atherosclerosis, hepatic and thyroid diseases.
Categories:
Price:
$49
|
|
Cholesteryl Esters, Serum
*Build Your Own Panel Eligible [?]
|
$310
|
|
Description:
- Check cholesterol storage and heart risk
- Monitor fat metabolism over time
- Track progress from diet changes
Categories:
Price:
$310
|
|
Cholinesterase, RBC and Plasma
*Build Your Own Panel Eligible [?]
|
$294
|
|
|
Description:
True cholinesterase (RBC and plasma) activity is decreased in individuals with exposure to organophosphorous insecticides. True cholinesterase, found in erythrocytes and nerve tissue, is responsible for inactivating acetylcholinesterase at nerve endings. With decreased enzyme activity, patients may display a range of nervous system dysfunction. Analysis of RBC and serum or plasma activity is useful in monitoring exposure and recovery.
Categories:
Price:
$294
|
|
Cholinesterase, Serum
*Build Your Own Panel Eligible [?]
|
$197
|
|
|
Description:
This test may be used to detect exposure to or poisoning from organophosphate-based pesticides; to assess baseline levels before exposure to organophosphates; or to monitor cholinesterase levels in individuals who work with pesticides. This test is also used in the diagnosis of inherited pseudocholinesterase deficiency, for individuals with a family history who will be receiving the muscle relaxant succinylcholine during surgery. The Cholinesterase, Serum assay is often used as part of the diagnostic evaluation for individuals who present with symptoms of pesticide poisoning. Symptoms of organophosphate poisoning can range from mild to severe and may include sweating, salivation, miosis, hypotension, urinary incontinence, mental confusion, gastrointestinal spasms, anxiety, insomnia, tremors, convulsions, respiratory depression, and circulatory collapse, among others [1]. This test is also used in the diagnosis of inherited pseudocholinesterase deficiency, an enzyme deficiency characterized by impaired metabolism of succinylcholine, a muscle relaxant for surgical anesthesia. Individuals with this disorder who receive succinylcholine are at risk for prolonged postsurgical apnea and paralysis lasting 2 or more hours [2]. Thus, testing may be helpful to evaluate individuals who present with these symptoms postsurgically, as well as those with a family history of pseudocholinesterase deficiency who are scheduled for surgery. References 1. Lessenger JE, Reese BE. J Am Board Fam Pract. 1999;12:307-314. 2. Soliday FK, et al. AANA J. 2010;78:313-320.
Categories:
Price:
$197
|
|
Cholinesterase, Serum, Plasma, RBC
*Build Your Own Panel Eligible [?]
|
$338
|
|
Description:
- Check chemical or pesticide exposure levels
- Monitor liver enzyme function easily
- Screen nerve and muscle function risks
Categories:
Price:
$338
|
|
Cholinesterase, Serum, with Dibucaine Inhibition
*Build Your Own Panel Eligible [?]
|
$318
|
|
|
Description:
The Pseudocholinesterase phenotype can be determined by analysis of Pseudocholinesterase and the percent inhibition by Dibucaine. Approximately 96% of the population has normal activity, approximately 4% will exhibit decreased activity that leads to prolonged paralysis following use of succinylcholine, and 1 in 3000 patients will exhibit severe, prolonged paralysis following anesthetic exposure.
Categories:
Price:
$318
|
|
Chromatin (Nucleosomal) Antibody
*Build Your Own Panel Eligible [?]
|
$324
|
|
|
Description:
Chromatin Antibody plays a central role in the autoimmune response in systemic lupus erythematosus (SLE). Approximately 90% of patients with SLE have sera that will exhibit reactivity to nucleosomes.
Categories:
Price:
$324
|
|
Chromium, 24-Hour Urine
*Build Your Own Panel Eligible [?]
|
$296
|
|
Description:
- Pinpoint chromium levels affecting your energy
- Reveal hidden factors behind blood sugar issues
- Clarify the cause of unexplained fatigue
Includes:
Creatinine
Categories:
Allergy blood testing,
Geriatrics/Age Management,
Neurology,
Pediatrics,
Price:
$296
|
|
Chromium, Blood
*Build Your Own Panel Eligible [?]
|
$119
|
|
|
Description:
This assay is useful to monitor exposure to chromium, progress of medical treatment or determine nutritional status.
Categories:
Price:
$119
|
|
Chromium, Fluid
*Build Your Own Panel Eligible [?]
|
$576
|
|
Description:
- Check chromium and metabolism balance
- Monitor blood sugar related fatigue
- Assess trace mineral nutrition levels
Categories:
Price:
$576
|
|
Chromium, Hair
*Build Your Own Panel Eligible [?]
|
$672
|
|
|
Description:
Exposure monitoring/investigation. Not for clinical diagnostic purposes.
Categories:
Price:
$672
|
|
Chromium, Nails
*Build Your Own Panel Eligible [?]
|
$672
|
|
|
Description:
Toxicity is mostly seen in occupational exposure.
Categories:
Price:
$672
|
|
Chromium, Plasma
*Build Your Own Panel Eligible [?]
|
$315
|
|
Description:
- Checks chromium levels in blood
- Monitors essential mineral for health
- Measures body's chromium balance
Includes:
Chromium, Plasma
Categories:
Price:
$315
|
|
Chromium, RBC
*Build Your Own Panel Eligible [?]
|
$352
|
|
Description:
- Checks chromium levels in blood cells
- Evaluates chromium inside red blood cells
- Measures chromium stored in RBCs
Includes:
Chromium, RBC
Categories:
Price:
$352
|
|
Chromium, Serum
*Build Your Own Panel Eligible [?]
|
$346
|
|
|
Description:
Occupational exposure and exposure to environmental contamination of chromium may lead to toxicity. The need for chromium supplements is unproven. Supplements taken in excess can lead to toxicity.
Categories:
Price:
$346
|
|
Chromium, Urine
*Build Your Own Panel Eligible [?]
|
$296
|
|
|
Description:
Occupational exposure and exposure to environmental contamination of chromium may lead to toxicity. The need of chromium supplements is unproven. Supplements taken in excess can lead to toxicity.
Includes:
Creatinine
Categories:
Allergy blood testing,
Geriatrics/Age Management,
Neurology,
Pediatrics,
Price:
$296
|
|
Chromogranin A, LC/MS/MS
*Build Your Own Panel Eligible [?]
|
$313
|
|
Description:
- Measures stress hormone levels
- Checks for certain tumor markers
- Assesses neuroendocrine activity
Includes:
Chromogranin A, LC/MS/MS
Categories:
Price:
$313
|
|
Chromosomal Microarray, Hematologic Malignancy, ClariSure® Oligo-SNP
*Build Your Own Panel Eligible [?]
|
$2985
|
|
|
Description:
To integrate the microarray in the investigation of neoplasms to assess genomic alterations and overall genomic complexity of the abnormal clone. To be used in conjunction with other established clinical laboratory tests for the malignancy in question.
Categories:
Price:
$2985
|
|
Chromosomal Microarray, POC, ClariSure® Oligo-SNP
*Build Your Own Panel Eligible [?]
|
$2985
|
|
|
Description:
Chromosomal microarray (CMA) detects aneuploidies, deletions and duplications below the resolution of chromosome analysis (karyotyping), and long continuous regions of homozygosity. Approximately 50% of first trimester pregnancy losses are due to chromosome abnormalities. While chromosome analysis on products of conception has an increased failure rate, chromosomal microarray is a DNA-based analysis, which rarely has assay failures.
Categories:
Price:
$2985
|
|
Chromosomal Microarray, POC FFPE, ClariSure® Oligo-SNP
*Build Your Own Panel Eligible [?]
|
$2985
|
|
|
Description:
This Oligo/SNP array assay of products of conception is used to detect genomic alterations that may be associated with fetal miscarriage and should be used in conjunction with conventional cytogenetics testing and clinical evaluation of the miscarriage.
Categories:
Price:
$2985
|
|
Chromosomal Microarray, Postnatal, ClariSure® Oligo-SNP
*Build Your Own Panel Eligible [?]
|
$4431
|
|
|
Description:
Chromosomal microarray (CMA) detects aneuploidies, deletions and duplications below the resolution of chromosome analysis (karyotyping), and long continuous regions of homozygosity. CMA analysis can help to determine genetic causes of developmental delay (DD), intellectual disability (ID), dysmorphic features, congenital anomalies and pervasive developmental disorders. This test can also be ordered on parents to determine if a copy number variant in a child is inherited or de novo.
Categories:
Price:
$4431
|
|
Chromosomal Microarray, Postnatal Familial Follow-up, ClariSure® Oligo-SNP
*Build Your Own Panel Eligible [?]
|
$1420
|
|
|
Description:
To assist in establishing the clinical significance when a relative's chromosomal microarray study reveals a copy number variant. This test determines the familial presence or absence of a specific CNV identified by chromosomal microarray testing in a proband.
Categories:
Price:
$1420
|
|
Chromosomal Microarray, Prenatal, ClariSure® Oligo-SNP
*Build Your Own Panel Eligible [?]
|
$2985
|
|
|
Description:
Chromosomal microarray (CMA) detects aneuploidies, deletions and duplications below the resolution of chromosome analysis (karyotyping), and long continuous regions of homozygosity. This assay may be useful for investigation of fetuses with abnormal ultrasound findings, abnormal prenatal screening, definition of unbalanced cytogenetic abnormalities, and follow-up to a documented chromosome or microarray abnormality in a sibling or a parent. Microarray analysis may also be used as follow up for a family history of a previous child with developmental delay, intellectual disability, and/or congenital malformations.
Categories:
Price:
$2985
|
|
Chromosomal Microarray, Solid Tumor FFPE, Clarisure® Oligo-SNP
*Build Your Own Panel Eligible [?]
|
$2985
|
|
|
Description:
To integrate the microarray in the investigation of neoplasms to assess genomic alterations and overall genomic complexity of the abnormal clone. To be used in conjunction with other established clinical laboratory tests for the malignancy in question.
Categories:
Price:
$2985
|
|
Chromosome Analysis,Amniotic Fluid Reflex to ClariSure®,Oligo-SNP,Prenatal
*Build Your Own Panel Eligible [?]
|
$1439
|
|
|
Description:
Testing determines chromosomal status of the fetus. Numerical and structural chromosomal abnormalities can be diagnosed. Sex and the presence of more than one cell line (mosaicism) can also be determined. Indications include diagnosis of chromosome abnormalities in fetuses of women who are of advanced maternal age; had a previous child with a chromosome abnormality; parental carrier of a balanced translocation, inversion or marker chromosome; parental mosaicism and follow-up for abnormal maternal serum alpha fetoprotein or maternal screening results. Chromosomal Microarray, Prenatal, ClariSure® Oligo-SNP - This assay may be useful for: • Further investigation on fetuses with abnormal ultrasound findings indicating congenital malformation. • Further definition of an imbalanced cytogenetic abnormality. • Further investigation on equivocal cytogenetic findings. • Attempt at characterization of supernumerary marker chromosome. • Follow-up to a documented chromosome abnormality or genomic alteration in a sibling or a parent. • Family history of a previous child with mental retardation and/or phenotypic abnormalities.
Categories:
Price:
$1439
|
|
Chromosome Analysis and AFP with Reflex to AchE, Fetal Hgb, and Oligo-SNP
*Build Your Own Panel Eligible [?]
|
$1535
|
|
|
Description:
Testing determines chromosomal status of the fetus. Numerical and structural chromosomal abnormalities can be diagnosed. Sex and the presence of more than one cell line (mosaicism) can also be determined. Indications include diagnosis of chromosome abnormalities in fetuses of women who are of advanced maternal age; had a previous child with a chromosome abnormality; parental carrier of a balanced translocation, inversion or marker chromosome; parental mosaicism and follow-up for abnormal maternal serum alpha fetoprotein or maternal screening results. Chromosomal Microarray, Prenatal, ClariSure® Oligo-SNP - This assay may be useful for: • Further investigation on fetuses with abnormal ultrasound findings indicating congenital malformation. • Further definition of an imbalanced cytogenetic abnormality. • Further investigation on equivocal cytogenetic findings. • Attempt at characterization of supernumerary marker chromosome. • Follow-up to a documented chromosome abnormality or genomic alteration in a sibling or a parent. • Family history of a previous child with mental retardation and/or phenotypic abnormalities.
Categories:
Price:
$1535
|
|
Chromosome Analysis and AFP with Reflex to AchE,Fetal Hgb,and Oligo-SNP(NY)
*Build Your Own Panel Eligible [?]
|
$1535
|
|
|
Description:
Testing determines chromosomal status of the fetus. Numerical and structural chromosomal abnormalities can be diagnosed. Sex and the presence of more than one cell line (mosaicism) can also be determined. Indications include diagnosis of chromosome abnormalities in fetuses of women who are of advanced maternal age; had a previous child with a chromosome abnormality; parental carrier of a balanced translocation, inversion or marker chromosome; parental mosaicism and follow-up for abnormal maternal serum alpha fetoprotein or maternal screening results. Chromosomal Microarray, Prenatal, ClariSure® Oligo-SNP - This assay may be useful for: • Further investigation on fetuses with abnormal ultrasound findings indicating congenital malformation. • Further definition of an imbalanced cytogenetic abnormality. • Further investigation on equivocal cytogenetic findings. • Attempt at characterization of supernumerary marker chromosome. • Follow-up to a documented chromosome abnormality or genomic alteration in a sibling or a parent. • Family history of a previous child with mental retardation and/or phenotypic abnormalities.
Categories:
Price:
$1535
|
|
Chromosome Analysis, Blood
*Build Your Own Panel Eligible [?]
|
$1227
|
|
Description:
- Checks for genetic problems in blood
- Looks for chromosome abnormalities
- Examines chromosomes for possible issues
Includes:
Chromosome Analysis, Blood
Categories:
Price:
$1227
|
|
Chromosome Analysis, Blood with reflex to Postnatal ClariSure® Oligo-SNP Array
*Build Your Own Panel Eligible [?]
|
$1281
|
|
|
Description:
Chromosome analysis can be used to help determine genetic causes of intellectual disability, developmental delay, congenital anomalies, infertility, miscarriage, stillbirth, and ambiguous genitalia. Chromosome analysis does not rule out cryptic or submicroscopic chromosome abnormalities. If this analysis is normal, microarray will be performed for the detection of submicroscopic deletions and duplications and long continuous regions of homozygosity.
Categories:
Price:
$1281
|
|
Chromosome Analysis, Chorionic Villus Sample
*Build Your Own Panel Eligible [?]
|
$1874
|
|
|
Description:
This test will detect chromosome abnormalities of the fetus including numerical, structural, and mosaic abnormalities. Chromosome analysis will also reveal fetal gender and sex chromosome abnormalities. Indications for prenatal chromosome analysis may include advanced maternal age, abnormal fetal ultrasound, abnormal maternal serum screen, abnormal cell-free DNA results, history of a previous child with a chromosome abnormality, or a parent who carries a balanced chromosomal rearrangement or has another chromosome abnormality.
Categories:
Price:
$1874
|
|
Chromosome Analysis,Chorionic Villus with Reflex to ClariSure®,Oligo-SNP,Prenatal
*Build Your Own Panel Eligible [?]
|
$1874
|
|
|
Description:
Testing determines chromosomal status of the fetus. Numerical and structural chromosomal abnormalities can be diagnosed. Sex and the presence of more than one cell line (mosaicism) can also be determined. Indications include diagnosis of chromosome abnormalities in fetuses of women who are of advanced maternal age; had a previous child with a chromosome abnormality; parental carrier of a balanced translocation, inversion or marker chromosome; parental mosaicism. Chromosomal Microarray, Prenatal, ClariSure® Oligo-SNP - This assay may be useful for: • Further investigation on fetuses with abnormal ultrasound findings indicating congenital malformation. • Further definition of an imbalanced cytogenetic abnormality. • Further investigation on equivocal cytogenetic findings. • Attempt at characterization of supernumerary marker chromosome. • Follow-up to a documented chromosome abnormality or genomic alteration in a sibling or a parent. • Family history of a previous child with mental retardation and/or phenotypic abnormalities.
Categories:
Price:
$1874
|
|
Chromosome Analysis, CLL/LPD
*Build Your Own Panel Eligible [?]
|
$1532
|
|
Description:
- Detect chromosome changes linked leukemia
- Monitor blood cancer disease progression
- Track genetic changes over time
Categories:
Price:
$1532
|
|
Chromosome Analysis, DEB Assay for Fanconi Anemia
*Build Your Own Panel Eligible [?]
|
$1406
|
|
|
Description:
This assay is a first-line screening test for patients with clinical suspicion of Fanconi anemia, an inherited disorder that causes chromosomal instability [1]. This test is not used to evaluate carrier status for Fanconi anemia or for prenatal testing.Fanconi anemia is a multigenic and primarily autosomal recessive disorder caused by pathogenic variants that affect DNA repair. Populations with increased carrier frequencies for 1 or more of these pathogenic variants include individuals of Ashkenazi Jewish, Afrikaner, sub-Saharan African, Roma, or South Asian (Indian and Pakistan) descent [1]. Clinical manifestations of Fanconi anemia vary broadly and may include congenital abnormalities, bone marrow failure, predisposition to cancer, and severe toxicity to chemotherapy. Early diagnosis is critical for patient management, especially in severe cases [1].This test evaluates chromosome breakage in cultured lymphocytes following treatment with diepoxybutane (DEB), a DNA cross-linking agent. Lymphocytes from patients with Fanconi anemia typically have an increased number of chromosomal breaks and aberrations. Clinical care guidelines for Fanconi anemia indicate that a positive test result should be followed by genetic testing to identify pathogenic variants; a negative test result with weak clinical suspicion may not require further testing; and an indeterminate (equivocal) result may be confirmed with a skin fibroblast chromosome breakage test [1].Although chromosome breakage analysis performed with peripheral blood is considered the gold standard for laboratory diagnosis of Fanconi anemia [1], other rare chromosome breakage disorders can also cause positive results. These include Nijmegen breakage syndrome, Roberts syndrome, and Warsaw breakage syndrome.The results of this test should be interpreted in the context of pertinent clinical and family history and physical examination findings.Reference1. Sroka I, et al, eds. Fanconi Anemia Clinical Care Guidelines. 5th ed. Fanconi Anemia Research Fund; 2020. Accessed April 19, 2022. https://www.fanconi.org/images/uploads/other/Fanconi_Anemia_Clinical_Care_Guidelines_5thEdition_web.pdf
Categories:
Price:
$1406
|
