We found 6 genetics specialists near Woodland Hills, CA.

Filter By:
Showing 1-6 of 6
Selecting one of the sort options will cause this page to reload and list providers by the selected sort order.

Specializes in Family Medicine, Public Health & General Preventive Medicine, Genetics
Average rating 5.0 stars out of 5 (2 ratings)
22636 Ventura Boulevard
Woodland Hills, CA

Dr. Claudia Mikail's areas of specialization are family medicine, public health & general preventive medicine, and genetics. Her areas of expertise include obesity, chromosomal disorders, and preventive care. She is affiliated with Providence Tarzana Medical Center and West Hills Hospital & Medical Center. Dr. Mikail's education and training includes medical school at Mount Sinai School of Medicine and residency at Columbia University Medical Center and a hospital affiliated with Stony Brook University Medical Center. Anthem, Blue Cross/Blue Shield, and Aetna are among the insurance carriers that Dr. Mikail takes. She welcomes new patients.

Read more

Clinical interests: Chromosomal Disorders, Preventive Care, Weight Management, Immigration Issues, Physical Exams, Obesi ... (Read more)

Specializes in Clinical Molecular Genetics, Clinical Cytogenetics
8401 Fallbrook Avenue
West Hills, CA

Specializes in Genetics
5601 De Soto Avenue; Third Floor--ob/gyn A
Woodland Hills, CA

Specializes in Genetics
5601 De Soto Avenue; Department of Genetics
Woodland Hills, CA

Specializes in Genetics, Geriatrics
23480 Park Sorrento; Suite 102b
Calabasas, CA

Specializes in Genetics
5601 De Soto Avenue
Woodland Hills, CA
What is Genetics?

Genetics is the branch of medicine dealing with the diagnosis, prevention, and treatment of genetically-linked or hereditary diseases. It includes both genetic counselors and medical geneticists, who may be involved in either patient care or research.

Medical geneticists are doctors who study genes and diseases that are caused by genes. There are many diseases linked to genetics, including:
  • 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.

Medical geneticists typically spend their career in research, although some treat or counsel patients. A patient may see a medical geneticist to obtain more information about their disorder or about how an inherited disorder might impact their family. The field of medical genetics includes the following four subspecialties:
  • 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.

Related to medical genetics is the field of genetic counseling. These healthcare professionals are not physicians, but they are educators who help patients interpret medical information about genetic risk, which can sometimes be difficult to understand or overwhelming. When families face the possibility of having a child with an inherited disease, genetic counselors educate them about their specific risks and options. They analyze patterns in family history and interpret the medical probability of a genetic disease occurring. They provide support and put families in contact with resources. Genetic counselors help families adapt to all of the implications that a hereditary disease can have in their life.
Selecting a checkbox option will refresh the page.