We found 6 genetics specialists who accept Bronze Choice HSA 6300 - 2 with IVF near Austin, TX.
Dr. Jaya George-Abraham, who practices in Austin, TX, is a medical specialist in pediatric genetics. Dr. George-Abraham has indicated that her clinical interests include genetic counseling. She is in-network for Blue Cross Blue Shield Bronze, Blue Cross Blue Shield HMO, and Blue Cross Blue Shield Gold, as well as other insurance carriers. Her education and training includes medical school at the University of Texas Health Science Center at San Antonio, School of Medicine and residency at a hospital affiliated with the University of Texas Southwestern Medical Center at Dallas. Dr. George-Abraham is affiliated with Seton Healthcare Family. She welcomes new patients.
Clinical interests: Growth Problems, Cognitive Problems, Genetic Counseling, Autism
Dr. Ladonna Immken specializes in pediatric genetics. Her education and training includes medical school at the University of Missouri-Columbia School of Medicine and residency at Jules Stein Eye Institute. In Dr. Immken's practice, she is particularly interested in genetic counseling. She is an in-network provider for Blue Cross/Blue Shield, Coventry, TRICARE, and more. She is professionally affiliated with Seton Healthcare Family. She is accepting new patients.
Clinical interests: Genetic Counseling
Dr. James Gibson works as a pediatric geneticist and clinical biochemical geneticist in Austin, TX. After attending Duke University School of Medicine, he completed his residency training at The Children's Hospital of Philadelphia. Dr. Gibson accepts several insurance carriers, including Blue Cross Blue Shield Bronze, Blue Cross Blue Shield HMO, and Blue Cross Blue Shield Gold. He is professionally affiliated with Seton Healthcare Family.
Dr. Thomas Hughes works as a pediatric geneticist in Austin, TX. Dr. Hughes is in-network for Aetna EPO, Blue Cross/Blue Shield, and Blue Cross Blue Shield Bronze, as well as other insurance carriers. He graduated from the University of Pittsburgh School of Medicine. He has received the distinction of Texas Super Doctors. He is professionally affiliated with Seton Healthcare Family.
Dr. Mathew Putzi is a medical specialist in molecular genetic pathology and cytopathology. Dr. Putzi (or staff) speaks Spanish and Vietnamese. He attended Tufts University School of Medicine and then went on to complete his residency at a hospital affiliated with the University of Michigan. United Healthcare Compass, United Healthcare Choice, and United Healthcare HSA are among the insurance carriers that Dr. Putzi honors.
Dr. Jose Garcia's medical specialty is clinical molecular genetics, general practice, and family medicine. He honors United Healthcare Compass, United Healthcare Choice, United Healthcare HSA, and more. He attended medical school at Baylor College of Medicine.
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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.