Genetics (clinical)
Genetic tests are done by analyzing small samples of blood or body tissues. They determine whether you, your partner, or your baby carry genes for certain inherited disorders.
Cook Children's clinical genetics offers evaluation and diagnosis of genetic disorders, as well as assists families with referrals to community resource services. The physicians and staff help patients and their families understand the disorders and related recurrence risks.
Our services
Each human being is made up of a unique set of chemical blueprints that contain our DNA. DNA makes up our genetic code. There are some 25,000 to 35,000 genes in each human being. Genes determine all kinds of things like hair and eye color, height, curly or straight hair, skin tone, and gender. Sometimes there is an error in a gene which can result in a birth defect or health issue. In some cases the genetic error becomes hereditary and passed on from parent to child. Knowing if a child's medical problems are genetic, or not, can help caregivers create a more accurate diagnosis and determine the best course of treatment. We offer a wide array of specialized genetic services, including:
- Gathering relevant birth, medical and developmental history of the patient, including their detailed family history.
- Clinical evaluation by a board certified geneticist.
- Relevant diagnostic testing.
- Detailed explanation of the diagnosis, prognosis and treatment options.
- Discussion of reproductive and recurrence risks.
- Psychosocial support.
- Referral to appropriate medical specialists and community resources.
- Communication with the patient’s primary care physician and related specialists.
Monthly Down syndrome clinics are available to help children and their caregivers understand and address unique needs and manage this diagnosis. Please call 682-885-2170 for more information.
