Vísað í erfðaheilbrigðisþjónustu
Að skilja niðurstöður erfðarannsókna
Upptökur (á ensku).
In this webinar, we discuss how to take a family history, effectively and systematically, to ensure you can identify patients at increased risk of a genetic condition.
In this webinar, we discuss how to record the family history, effectively and systematically, using accepted pedigree symbols. You will have the chance to practice yourself.
The common inheritance patterns are explained, along with the risks to family members if a patient is diagnosed with a genetic condition.
In this webinar, we discuss the various types of prenatal tests, including population screening and specific tests to identify a fetus at high risk of a genetic condition known to be in the family.
New non-invasive tests using cell-free fetal DNA (NIPT) are covered.
In this webinar, we discuss the types of genetic tests that might be offered to your patient and the possible results, to help you explain those.
Would you know who to refer to genetic services, or how to find those services? In this webinar we discuss types of patients who benefit from referral and how you can identify where to refer.