Does your child have a medical condition, developmental, physical or neurological problem for which medical specialists do not know the cause? Our genetic counselling service is for consulting couples whose child is suspected of having a genetic disease.
What is the purpose of genetic counselling?
If a child’s general practice specialist diagnostic tests fail to identify the origin of the problem, there may often be a genetic disease. This can be a hereditary problem or a so-called “de novo” or newly developing disorder.
During a genetic counselling session, the clinical geneticist will first review the family history with the parents and then examine the child. Then, if the doctor deems it appropriate, a genetic screening test may be recommended. A number of different panel tests are available at our Centre, from which the doctor will choose the most appropriate test. The results of these screenings are also evaluated during a consultation, and if the result is positive, the parent will receive a recommendation for further action.
The specific risk of recurrence is determined, and the specific risk level is then established. Where possible, therapy is sought if there is a specific therapy for the condition. In the case of repeat offspring of the parents of the affected person, the method of prenatal diagnosis, i.e. fetal examination, is selected and organised. Summary counselling is provided during this process.
