We found 6 genetics specialists who accept Silver Compass 4000 near Miami, FL.
Dr. Deborah Barbouth is a Miami, FL physician who specializes in pediatric genetics. She takes several insurance carriers, including Blue Cross Blue Shield EPO, Blue Cross Blue Shield Bronze, and Blue Cross Blue Shield HMO. Awards and/or distinctions Dr. Barbouth has received include Florida Super Doctors 2009 - South Florida Edition and Florida Super Doctors. Dr. Barbouth (or staff) speaks Hebrew and Spanish. Dr. Barbouth is affiliated with Broward Health Medical Center.
Dr. Stephanie Sacharow works as a genetics specialist in Miami, FL. United Healthcare HMO, United Healthcare Compass, and United Healthcare Navigate are among the insurance carriers that Dr. Sacharow honors.
Dr. Mustafa Tekin sees patients in Miami, FL. His medical specialty is genetics. He is an in-network provider for Blue Cross Blue Shield EPO, Blue Cross Blue Shield Bronze, Blue Cross Blue Shield HMO, and more.
Dr. Brocha Tarshish practices genetics and obstetrics & gynecology. She is an in-network provider for Blue Cross Blue Shield EPO, Blue Cross Blue Shield Bronze, and Blue Cross Blue Shield HMO, as well as other insurance carriers. She obtained her medical school training at Tel Aviv University, Sackler Faculty of Medicine and performed her residency at North Shore University Hospital and a hospital affiliated with Emory University. Dr. Tarshish is professionally affiliated with Broward Health Medical Center.
Dr. Yao-Shan Fan is a genetics specialist. Dr. Fan accepts Blue Cross/Blue Shield, Blue Cross Blue Shield Bronze, and Blue Cross Blue Shield HMO, in addition to other insurance carriers.
Medicare Patient Age
Medicare Patient Conditions
Medicare Patient Ethnicity
Medicare Patient Gender
Medicare Patient Insurance Eligibility
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.