Our genetic counseling team can meet with patients for a variety of indications. Some patients may have a long-standing clinical diagnosis suspicious for an underlying genetic cause. Examples include, but certainly are not limited to, polycystic kidney disease, bilateral sensorineural hearing loss, and pulmonary fibrosis.
Our genetic counselors clarify genetic risk by reviewing each patient’s medical history in addition to taking a thorough family history. They have specialized training to be able assess and explain genetic risks, reproductive risks, and patient testing options. They also have expertise in interpreting and explaining genetic testing results and limitations, helping both patients and non-genetics providers understand the implications.
In cases where a genetic cause for a diagnosis is identified, our genetic counselors will also help with identifying and communicating with at-risk family members.
What to Expect:
A genetic counselor identifies genetic risk by reviewing each patient’s medical history in addition to taking a thorough family history. They have specialized training to be able assess and explain genetic risks, patient testing options, in addition to interpreting and describing genetic testing results in an understandable manner.
A genetic counselor will not require you to have any testing you do not want. Rather, a genetic counselor will provide you with complete information about testing options so you can make decisions that are right for you and your family.
Meet our Team:
More Information and Scheduling:
We recommend first talking with your doctor about your health condition; if appropriate, they can refer you to our program. If you have further questions about meeting with one of our genetic counselors, please reach out to our Genetics Program: (414) 955-4254.