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Keywords
- ABPA_Aspergillus
- accompanying diseases
- air-improving devices
- allergy
- animals_pets
- antibiotic therapy
- asthma
- complementary medicine
- covid-19
- diabetes
- diagnostics
- drugs side effects
- drugs under development_genetic therapy
- ENT
- general aspects
- genetics
- health care
- hepatobiliary disease
- hygiene
- i.v.-lines
- inhalation
- lung
- microbiology
- miscellaneous
- modulator therapy
- MRSA
- nutrition and GI problems
- oxygen supplementation_therapy
- physiotherapy
- Pseudomonas aeruginosa
- psychosocial
- public facilities
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- reproduction
- research
- social law
- sport
- swine flu_novel influenza
- transplantation
- travelling
- vaccination
- ventilation
Topics
- CF test for only one parent
- Hello, I would like to know the impact on my 5-year and 6-months-old daughter’s health who was F508del homozygous diagnosed in 2011. Regarding that only her mother has made genetic testing (her father did not wish to do), could you give me some information about it and whether it will affect ...
- 04.11.2014
- Mutation delta f508/2789+5g a
- My daughter has an atypical form of CF with the mutations delta F508 / 2789+5G>A. Do you have any experience with the mutation? What does atypical mean?
- 03.11.2014
- R1162X and Q1035X
- Hello dear expert team, recently, the mutations R1162X and Q1035X have been detected in my genetic material. Could you please answer the following questions about this combination: - Is there a prognosis concerning the course of the illness? - How is the frequency of both mutations ...
- 03.11.2014
- Prognosis of mutation classes
- Dear experts, I am always told that the prognosis for CF patients can never be predicted, that it is very different from patient to patient. It would depend on the genes and also on other factors. This is what I know - but as a parent of a CF child one is of course tortured by the insecurity if ...
- 20.10.2014
- CT scan of the lungs appropriate?
- Hello, many thanks for your help in advance! Age: 36, male, in the frame of a genetic investigation at a center for reproductive medicine a genetic defect has been detected (before history of hypozoospermia, infertility diagnostics in case of CFTR-related disorder). Bronchial asthma, allergic ...
- 29.09.2014
- Suspicion of CF
- Hello on your site again, Still with not that many answers to my questions regarding the diagnosis of my child who is now 15 years old. I'd like your opinion, my son is pancreatic insufficient, so he takes Creon. He had 3 sweat tests all positive, but the genetic test is negative!! He has a ...
- 15.09.2014
- p.F508del
- Hello, We just received the two mutations of our daughter. The p.F508del and c.3140-26A> G (3272-26A> G) Please, what will be the common impacts of these changes even though I know it varies from one individual to another? Thank you in advance for your help and feedback.
- 10.09.2014
- CF mutation
- Hello, can you explain what does it mean that the F508del mutation of the CFTR gene has been found in my 5.5 year-old daughter, and what are the consequences for her respiratory as well digestive health? Thank you
- 10.09.2014
- G542X
- G542X heterozygous mutation and polymorphisms 7T and 9T from a villous biopsy- does this mean a healthy carrier status? (Given that I have a child with the mutations G542X and deltaF508 heterozygous)
- 29.07.2014
- Hello
- I have one-year-old boy diagnosed with cystic fibrosis at 6 months. We did the genetic test and the result was: M - G 542X heterozygous; 9T. Child‘s doctor says that the outcome would be a milder disease and he does not believe he will have major problems in the future. But another doctor said ...
- 15.09.2014