Services

All Lab Tests & Services

Our services include all areas of Anatomical and Clinical Pathology, such as Hematology, Chemistry, Serology, Toxicology, Molecular Testing in Microbiology, Genetics of Cancer-Risk, Surgical Pathology and Cytopathology.

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Pathology Services

In Services

SMA Laboratory performs a full range of high quality Anatomic Pathology and Non-Gyn Cytopathology services, including histopathology, liquid-based non-gyn cytology, special stains, and immunohistochemistry.

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Toxicology Services

In Services

Our Toxicology department provide SMA clients with drug monitoring expertise for patients in need for prescription medications. This service has expanded to include illicit drug of abuse testing.

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Genetic Testing

In Services

Our Genetic testing identifies changes in chromosomes, genes, or proteins. These results can confirm or rule out a suspected genetic condition or help determine a person’s chance of developing or passing on a genetic disorder.

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Molecular Microbiology

In Services

At SMA, we provide vigorous testing for Viral Targets, Bacterial Targets through various methods including respiratory, gastrointestinal, urinary tests, wounds, and vaginal.

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Life Wellness Program

In Services

SMA provides cognitive wellness testing to provide personalized medicine for individual improvement. Early diagnosis empowers individuals and families more time to plan.

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Covid-19 PCR & Antibody

In Services

High-throughput, automated testing that utilizes RT-PCR & detection of antibodies in the blood that are produced by the body in response to SARS-CoV-2 virus or after vaccination

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Routine Microbiology

In Services

The Clinical Microbiology Laboratory at SMA offers full-service diagnostic testing in bacteriology and molecular epidemiology. Our laboratory provides timely, accurate, and medically relevant results to aid in the evaluation, diagnosis, and treatment of infectious diseases

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ComprehensiveDx Clear™

ComprehensiveDx Clear™
Test Code:	1248
Test Description	ComprehensiveDx Clear is a comprehensive panel for hereditary breast, ovarian, uterine, colorectal, pancreatic, prostate and melanoma cancers.
Genes Tested	GENE	ASSOCIATED CANCER(S)	SYNDROME
	APC	Colorectal, pancreatic and other	Familial Adenomatous Polyposis syndrome, Gardner syndrome, and Turcot syndrome
	ATM	Breast, pancreatic	Ataxia-telangiectasia (if both copies of the gene are mutated)
	BAP1	Renal, melanoma, mesothelioma	Familial Melanoma Cancer Syndrome
	BARD1	Breast, ovarian
	BMPR1A	Colorectal, gastric, pancreatic	Juvenile Polyposis syndrome
	BRCA1	Breast, ovarian, pancreatic, prostate, male breast	Hereditary Breast and Ovarian Cancer syndrome
	BRCA2	Breast, ovarian, pancreatic, prostate, male breast, melanoma	Hereditary Breast and Ovarian Cancer syndrome;
	BRCA2		Fanconi anemia (if both copies of the gene are mutated)
	BRIP1	Ovarian, breast	Fanconi anemia (if both copies of the gene are mutated)
	CDH1	Breast, gastric, colorectal	Hereditary Diffuse Gastric Cancer
	CDK4	Melanoma, pancreatic	Familial Melanoma Cancer Syndrome
	CDKN2A	Melanoma, pancreatic	Familial Melanoma Cancer Syndrome
	CHEK2	Breast, colorectal
	DICER1	Lung, kidney, thyroid, ovarian
	EPCAM	Colorectal, gastric, endometrial, ovarian	Lynch (Hereditary non-polyposis colon cancer) syndrome
	FANCC	Breast	Fanconi anemia (if both copies of the gene are mutated)
	MRE11A	Breast, ovarian	Ataxia-telangiectasia-like Syndrome (if both copies of the gene are mutated)
	MSH2	Colorectal, gastric, endometrial, ovarian	Lynch (Hereditary non-polyposis colon cancer) syndrome
	MSH6	Colorectal, endometrial	Lynch (Hereditary non-polyposis colon cancer) syndrome
	MUTYH	Colorectal	MUTYH-associated Polyposis syndrome
	NBN	Breast, melanoma, prostate	Nijmegen breakage syndrome (if both copies of the gene are mutated)
	PALB2	Breast, ovarian, pancreatic, male breast	Fanconi anemia (if both copies of the gene are mutated)
	PMS2	Colorectal, endometrial, gastric, ovarian	Lynch (Hereditary non-polyposis colon cancer) syndrome
	POLD1	Colorectal, endometrial	Familial Adenomatous Polyposis syndrome
	POLE	Colorectal, gastrointestinal	Familial Adenomatous Polyposis syndrome
	PTEN	Breast, uterine, colorectal, thyroid, kidney, melanoma	Cowden Syndrome / PTEN Hamartoma Tumor Syndrome
	RAD50	Ovarian
	RAD51C	Breast, ovarian	Fanconi anemia (if both copies of the gene are mutated)
	RAD51D	Breast, ovarian
	SDHA	Gastrointestinal, other	Paragangliomas 5
	SDHB	Gastrointestinal, renal, other	Paraganglioma and gastric stromal sarcoma
	SDHC	Gastrointestinal, renal, other	Paraganglioma and gastric stromal sarcoma
	SDHD	Gastrointestinal, renal, other	Cowden Syndrome 3; Paraganglioma and gastric stromal sarcoma
	SMAD4	Colorectal, gastric	Juvenile Polyposis syndrome
	STK11	Colorectal, endometrial, gastric, ovarian, breast, pancreatic	Peutz-Jeghers syndrome
	TP53	Colorectal, breast, pancreatic, sarcomas, gastrointestinal, adrenocortical, leukemia	Li-Fraumeni syndrome
Specimen Requirements	Blood (two 4ml EDTA tubes, lavender top) or Extracted DNA (3ug in EB buffer) or Buccal Swab or Saliva (kits available upon request)
Turnaround Time (TAT)	2-3 weeks

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BreastDx Clear™

BreastDx Clear™
Test Code:	1250
Test Description	BreastDx Clear is a multi-gene test that analyzes 16 breast cancer susceptibility genes. Although all women have some risk of developing breast and/or ovarian cancer at some point in their lives, having a mutation in one of the breast cancer susceptibility genes increases this risk. Men who have a mutation in one of the breast cancer susceptibility genes have an increased risk of breast, prostate, pancreatic, gastric and other cancer types.
Genes Tested	GENE	ASSOCIATED CANCER(S)	SYNDROME
	ATM	Breast, pancreatic	Ataxia-telangiectasia (if both copies of the gene are mutated)
	BARD1	Breast, ovarian
	BRCA1	Breast, ovarian, pancreatic, prostate, male breast	Hereditary Breast and Ovarian Cancer syndrome
	BRCA2	Breast, ovarian, pancreatic, prostate, male breast, melanoma	Hereditary Breast and Ovarian Cancer syndrome;
			Fanconi anemia (if both copies of the gene are mutated)
	BRIP1	Ovarian, breast	Fanconi anemia (if both copies of the gene are mutated)
	CDH1	Breast, gastric, colorectal	Hereditary Diffuse Gastric Cancer
	CHEK2	Breast, colorectal
	FANCC	Breast	Fanconi anemia (if both copies of the gene are mutated)
	MRE11A	Ovarian, breast	Ataxia-telangiectasia-like Syndrome (if both copies of the gene are mutated)
	NBN	Breast, melanoma, prostate	Nijmegen breakage syndrome (if both copies of the gene are mutated)
	PALB2	Breast, ovarian, pancreatic, male breast	Fanconi anemia (if both copies of the gene are mutated)
	PTEN	Breast, uterine, colorectal, thyroid, kidney	Cowden Syndrome / PTEN Hamartoma Tumor Syndrome
	RAD51C	Breast, ovarian	Fanconi anemia (if both copies of the gene are mutated)
	RAD51D	Breast, ovarian
	STK11	Breast, ovarian, colorectal, gastric, pancreatic	Peutz-Jeghers Syndrome
	TP53	Breast, brain, sarcomas, gastrointestinal, adrenocortical, leukemia	Li-Fraumeni Syndrome
Specimen Requirements	Blood (two 4ml EDTA tubes, lavender top) or Extracted DNA (3ug in EB buffer) or Buccal Swab or Saliva (kits available upon request)
Turnaround Time (TAT)	2-3 weeks

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ColoDx Clear™

ColoDx Clear™
Test Code:	1251
Test Description	Colorectal cancer is the fourth most common type of cancer diagnosed in the United States and the second leading cause of cancer-related deaths in the country. ColoDx Clear is a multi-gene test focused on hereditary colon cancer syndromes. Pathogenic variants (mutations) in high-risk colorectal cancer genes are associated with several hereditary cancer syndromes and increase the risk of cancer in many organs.
Genes Tested	GENE	ASSOCIATED CANCER(S)	SYNDROME
	APC	Colorectal, pancreatic and other	Familial Adenomatous Polyposis syndrome, Gardner syndrome, and Turcot syndrome
	BMPR1A	Colorectal, gastric	Juvenile Polyposis syndrome
	EPCAM	Colorectal, gastric, endometrial, ovarian	Lynch (Hereditary non-polyposis colon cancer) syndrome
	MLH1	Colorectal, gastric, endometrial, ovarian	Lynch (Hereditary non-polyposis colon cancer) syndrome
	MSH2	Colorectal, gastric, endometrial, ovarian	Lynch (Hereditary non-polyposis colon cancer) syndrome
	MSH6	Colorectal, endometrial	Lynch (Hereditary non-polyposis colon cancer) syndrome
	MUTYH	Colorectal	MUTYH-associated Polyposis syndrome
	PMS2	Colorectal, endometrial, gastric, ovarian	Lynch (Hereditary non-polyposis colon cancer) syndrome
	POLD1	Colorectal, endometrial	Familial Adenomatous Polyposis syndrome
	POLE	Colorectal, gastrointestinal	Familial Adenomatous Polyposis syndrome
	PTEN	Colorectal, endometrial, breast, melanoma	Cowden syndrome
	SMAD4	Colorectal, gastric	Juvenile Polyposis syndrome
	STK11	Colorectal, endometrial, gastric, ovarian, breast, pancreatic	Peutz-Jeghers syndrome
	TP53	Colorectal, breast, pancreatic and other	Li-Fraumeni syndrome
Specimen Requirements	Blood (two 4ml EDTA tubes, lavender top) or Extracted DNA (3ug in EB buffer) or Buccal Swab or Saliva (kits available upon request)
Turnaround Time (TAT)	2-3 weeks

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ProstateDx Clear™
Test Code:	1257
Test Description:	The ProstateDx Clear™ Panel examines genes associated with an increased risk for prostate cancer. This test includes both well-established prostate cancer susceptibility genes, as well as candidate genes with limited evidence of an association with prostate cancer.
Genes Tested:	ATM, BRCA1, BRCA2, CHEK2, EPCAM, HOXB13, MLH1, MSH2, MSH6, NBN, PALB2, PMS2, TP53
Specimen Requirements	Blood (two 4ml EDTA tubes, lavender top) or Extracted DNA (3ug in EB buffer) or Buccal Swab or Saliva (kits available upon request)
Turnaround Time (TAT)	2-3 weeks

SMA Specialty Medical Lab – Services Overview

ComprehensiveDx Clear™

BreastDx Clear™

ColoDx Clear™

ProstateDx Clear™