We found 4 genetics specialists who accept Medicare near Chantilly, VA.
Dr. Celeste Riley is a molecular genetic pathology, pediatric pathology, and cytopathology specialist. Dr. Riley is an in-network provider for Medicare insurance. She studied medicine at Penn State College of Medicine. Dr. Riley (or staff) is conversant in Spanish, French, and Cantonese.
Dr. Daniel Jones is a molecular genetic pathologist and hematopathologist. Dr. Jones has a special interest in health informatics. He attended Case Western Reserve University School of Medicine and subsequently trained at Brigham and Women's Hospital and a hospital affiliated with Harvard Medical School for residency. He is an in-network provider for Medicare insurance. Awards and/or distinctions he has received include **Also Board Certified in Molecular Genetic and Pathology**. Dr. Jones is not currently accepting new patients.
Clinical interests: Health Informatics
Dr. Ozlem Goker-Alpan practices clinical biochemical genetics. In addition to English, Dr. Goker-Alpan (or staff) speaks Arabic, Spanish, and Hindi. In her practice, Dr. Goker-Alpan focuses on genetic issues and general care. Her hospital/clinic affiliations include Inova Fair Oaks Hospital and Inova Fairfax Hospital. After attending Marmara University School of Medicine, she completed her residency training at a hospital affiliated with Marmara University and a hospital affiliated with Stony Brook University Medical Center. Dr. Goker-Alpan is an in-network provider for Medicaid and Medicare insurance.
Clinical interests: Genetic Issues, General Care
Dr. Carla Macleod is a molecular genetic pathology and cytopathology specialist. Dr. Macleod takes MAMSI, Coventry, Cigna, and more. She graduated from Autonomous University of Barcelona Faculty of Medicine and the University of Barcelona Faculty of Medicine. For her professional training, Dr. Macleod completed a residency program at Washington Hospital Center. Dr. Macleod (or staff) speaks Filipino, Spanish, and French.
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- Single gene disorders, the result of a single mutated gene. Examples include Huntington’s disease, which causes jerky movements, and sickle-cell anemia, where red blood cells have an abnormal, rigid shape.
- Inborn metabolic disorders, which are a specific type of single gene disorder that results in abnormalities in the way the body chemically processes proteins, carbohydrates or fats. Some examples are Urea Cycle Disorder (where ammonia builds up in the body) and Gaucher’s Disease (where fatty substances build up in cells and organs).
- Chromosomal disorders, where gene-carrying chromosomes do not pair up correctly or are missing. Some examples are Klinefelter Syndrome, a sex-chromosome disorder, and Down Syndrome.
- Congenital abnormalities (commonly known as birth defects), which can be caused by genetic abnormalities. They also can happen because of illness or environmental exposure during pregnancy (such as with rubella), or for unknown reasons.
- Other common diseases that have hereditary traits, such diabetes, autism, and some types of cancer.
- Clinical Genetics: This overarching branch of medical genetics deals with the treatment and management of hereditary diseases.
- Biomechanical Genetics: This branch deals with metabolic disorders, such as galactosemia and phenylketonuria.
- Cytogenetics: This specialty deals with chromosomes and their associated diseases, as well as testing their structure and number.
- Molecular Genetics: This specialty focuses on DNA, interpreting DNA sequencing and other tests, and relating DNA information to specific diseases.