i
Loading Page
loading, please wait

Filters

FILTERS

Clear All Filters

GENDER

CONDITIONS / TREATMENTS

Search for Conditions/Treatments...

PRACTICE AFFILIATIONS

Search for Practice Affiliations...

SPECIALTIES

SORT BY

Molecular Genetic Pathologist - Syracuse, NY

We found 4 molecular genetic pathologist in Syracuse, NY. See refinement options below.

Sort By
  • Default
  • Patient Rating
  • Distance

Related searches

You can further refine your search:

intraoperative pathology consultation (3) , cytology (3) , lab tests (3) , slide consultation (2) , screening psa test (1)

Other Providers in Syracuse, NY

Addiction Doctors: Specialists & Psychiatrists Audiologists Child Psychologists Chiropractors Family Physicians & Family Medicine Specialists Holistic Doctors & Alternative Medicine Doctors Neuroradiologists Obstetricians & Gynecologists: OB-GYNs Occupational Therapists Pediatric Otolaryngologists / Ear, Nose & Throat Doctors Prosthodontists Radiation Oncologists Rehabilitation Physicians Surgical Dermatologists Urgent Care Doctors

What is Molecular Genetic Pathology?

Molecular genetic pathology is a medical specialty that integrates pathology and genetics to diagnose, analyze, and monitor genetic disorders. This specialty is critical to understanding why certain people acquire or are born with certain health conditions. Molecular genetic pathologists sequence and assess patients' nucleic acids (DNA and RNA) and look for mutations that signal the presence or risk of inherited genetic diseases like cystic fibrosis or sickle cell anemia. Molecular genetic pathologists can detect these potential genetic abnormalities, such as trisomy (extra chromosome) and monosomy (missing chromosome). Molecular genetic pathologists are physicians with additional training in pathology and molecular genetics and generally work in a laboratory using advanced equipment and technology. Conditions which a molecular genetic pathologist may diagnose include:

  • Developmental conditions
  • Tumors
  • Leukemia and lymphomas
  • Hematologic (blood) disorders
  • Pharmacogenetics (drug reactions or sensitivities)
  • Inherited and infectious diseases

Children and adults may be asked to submit blood or cheek swab specimens for analysis by a molecular genetic pathologist. Molecular genetic pathologists also perform prenatal diagnostic tests or screenings to determine if an infant has or is at risk for a condition. This helps caregivers prepare and care for their baby before birth. Genetic pathologists may use the following:

  • Fluorescence in situ hybridization (FISH) tests, which can identify genetic fragments of disease
  • Polymerase chain reaction (PCR) amplification, which can make and enlarge copies of DNA
  • CRISPR technology, which can identify parts of DNA in a cell

After a test is completed, molecular genetic pathologists can interpret test results and advise patients on risk, prevention, and treatment options. Molecular genetic pathologists may collaborate with cytogeneticists, hematopathologists, clinical pathologists, geneticists, and hematologists.