Nemours

Genetics

Thanks to advances in medical research, doctors now have the tools to understand how certain illnesses, or increased risks for certain illnesses, pass from generation to generation. Genetic services at Nemours include providing families with information related to the thousands of known diseases that may be hereditary in origin, as well as the evaluation, diagnosis, genetic counseling, and treatment of genetic disorders.

A typical evaluation includes taking a medical history, developmental history, family history, and performing a physical examination. In many cases these histories are supplemented by laboratory tests (for example, chromosome analysis), diagnostic studies (for example, computed tomography scanning (CT), or magnetic resonance imaging (MRI) scans), and referral to other subspecialty clinics (for example, ophthalmology, neurology, or orthopedics).

After this diagnostic evaluation has been completed, education and counseling can be provided regarding the history of the condition, as well as its prognosis, treatment, and risk of recurrence.

Nemours geneticists are usually trained in multiple specialties—pediatrics and genetics, for example. Nemours geneticists use an integrated medical record that unifies patient care across specialties and locations, prompting geneticists to consider best practices gained from Nemours experience and academic literature. We provide excellent care that places the patient and family at the center, and our commitment to communication is central to the process. We strive to create a uniquely satisfying experience bringing peace of mind to patients and families.

Nemours locations offer a range of genetic services. Please refer to the sites listed to the left for specific services available at each location.