We found 4 genetics specialists who accept Humana Silver HMO near Tampa, FL.
Dr. Amarilis Sanchez-Valle is a specialist in pediatric genetics. She works in Tampa, FL. Her clinical interests include metabolism. Dr. Sanchez-Valle's hospital/clinic affiliations include St. Joseph's Hospital, the University of South Florida (USF) Health, and St. Joseph's Women's Hospital. She attended the University of Puerto Rico School of Medicine and then went on to complete her residency at a hospital affiliated with the University of Texas Health Science Center at Houston and a hospital affiliated with Baylor College of Medicine. She takes Blue Cross Blue Shield EPO, Blue Cross Blue Shield Bronze, and Blue Cross Blue Shield HMO, as well as other insurance carriers. Dr. Sanchez-Valle has received the following distinctions: Medical Biochemical Genetics Board Certification, American Board of Medical Genetics and Genomics; Clinical Genetics Board Certification, American Board of Medical Genetics and Genomics; and Pediatrics Board Certification, American Board of Pediatrics. She is accepting new patients.
Clinical interests: Metabolism
Dr. Judith Ranells is a physician who specializes in pediatric genetics. Dr. Ranells graduated from Howard University College of Medicine. Her medical residency was performed at a hospital affiliated with Albert Einstein College of Medicine. These areas are among her clinical interests: genetic counseling and metabolism. Dr. Ranells is in-network for several insurance carriers, including Blue Cross Blue Shield EPO, Blue Cross Blue Shield Bronze, and Blue Cross Blue Shield HMO. She is affiliated with the University of South Florida (USF) Health. Her practice is open to new patients.
Clinical interests: Genetic Counseling, Metabolism
Dr. Kathleen Pope sees patients in Tampa, FL. Her medical specialty is genetics. She is an in-network provider for Blue Cross Blue Shield EPO, Blue Cross Blue Shield Bronze, Blue Cross Blue Shield HMO, and more. She studied medicine at Indiana University School of Medicine.
Conditions / Treatments
Years Since Graduation
- 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.