Genetic Clinic "Rajská zahrada"
The medical genetics clinic provides genetic counselling to families and individuals carrying a potentially hereditary disease. Genetic consultation is also part of the diagnosis of possible causes of fertility disorders.
The aim of genetic counselling is to determine the level of risk of a genetic disease, or to diagnose a genetic disease in an individual or a fetus and to suggest a further course of action. In the case of sex cell donors, genetic counselling and subsequent specialised genetic testing eliminates the risk of transmission of genetic conditions.
Consultation with a doctor (clinical geneticist) is covered by public health insurance. For uninsured clients we can offer a consultation under the self-payment scheme.
Genetic counselling is based on communication between the clinical geneticist and the client. If you are concerned about the possible genetic burden of your or your offspring, then it is advisable to discuss these concerns with a specialist.
The purpose is to provide the client with all the relevant information regarding their genetic burden, explain the results of the tests carried out so far, find possible causes of the disease and treatment options, but most importantly determine the risks of recurrence of the disease in offspring, or suggest measures to reduce these risks. The patient’s consent is required for all genetic tests and possible interventions.
Your GP or gynaecologist will make a recommendation for a genetic consultation. In some cases it is possible to have a consultation without a doctor’s recommendation.
It is important to note that any information you provide as part of a genetic consultation is confidential. The clinical geneticist will inform you of the findings in a strictly non-directive manner. He or she may recommend further tests and suggest measures to help resolve your situation. It is the inalienable right of the consulted person or couple to decide freely on the proposed course of action. It is important to remember that all information you provide in the genetic consultation is confidential. The clinical geneticist will inform you of the findings in a strictly non-directive manner. He or she may recommend further tests and suggest measures to help resolve your situation. It is the inalienable right of the consulted person or couple to decide freely on the proposed course of action.
The genetic diagnosis is based on the client’s medical records, clinical and genetic examinations, or examinations of the extended family. If necessary, a number of specialised genetic tests can be performed in our accredited laboratory. Once a diagnosis (even a probable one) has been made, the clinical geneticist will inform you clearly about the genetic prognosis and possible risks. It is important that the information conveyed is understandable to the client, especially if it leads to a major decision. The doctor must always accept this decision.
Before or during the genetic consultation it is necessary to fill in the Genetic Testing Questionnaire. You can download the questionnaire form in the link below or in the Downloads section, or pick it up in person at the GENvia outpatient clinic at any time during office hours. You can fill in the documents for the genetic consultation in the comfort of your own home. If you do not use this option, you will receive and complete the questionnaire during the genetic consultation.
Here is a brief overview of clients for whom the genetic consultation is suitable:
- Partners with positive anamnesis (infertility, sterility of unknown aetiology, repeated abortions, congenital malformations, hereditary diseases in the family)
- Partners prior to artificial insemination
- Sperm and oocytes donors by IVF
- Investigation of blood-related partners, kinship marriages
- Families with the incidence of cancer in several generations or by a child
- Families with the incidence of cystic fibrosis
- Families with the incidence of congenital anomalies or suspected hereditary diseases
- Persons with hereditary tendency to thrombosis (thrombophilia mutation testing)
- Persons with bone dysplasia, small or excessive growth
- Children with precocious or delayed puberty or genital developmental defects
- Children with psychomotor retardation
- Pregnant women with pathologic findings in biochemical screening or ultrasound findings
- Pregnant women over 35 years at time of delivery
- Influence assessment of mutagens (work in high-risk premises, the state after cytostatic treatment)
Hours of attendance
Tuesday | 11:00-17:00 |
Friday | 11:00-17:00 |
Contact
Head doctor: | MUDr. Kamila Světnicová |
Phone: | 777 669 470 |
E-mail: | ambulance@genvia.cz |
Note 1: To make an appointment with the doctor in our genetic outpatient clinic, please use preferentially the e-mail, in which will be stated the reason for the consultation, the name and the contact phone number.
Note 2: Before your visit of the outpatient clinic fill out the following questionnaire.
Location of the clinic
The genetic ambulance is located in Prague 9, at the metro station of line B “Rajská zahrada”, in the area of the polyclinic – entrance from Černičná street.
How to reach us by the public transport
How to reach us by car
Arrival to the polyclinic with subsequent parking in front of the polyclinic or in neighbouring streets.