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Tags
- 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
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- swine flu_novel influenza
- transplantation
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- vaccination
- ventilation
Topics
- Aspergillis
- The aspergillis requires a heavy treatment. Are there scientific studies into the effectiveness and consequences of la (long-term) treatment with anti-fungal medication?
- 22.06.2018
- distended gallbladder and hyperechogenic bowel
- Our second baby (I am 20 weeks pregnant) was diagnosed with distended gallbladder and hyperechogenic bowel. Are these two connected, or not? Could you give us some information about the first, which is somewhat rare? Is amniocentesis advisable?
- 22.06.2018
- Combination of DF508/R1162L
- After testing I was found to carry the c.3485G>(R1162L) mutation and my husband the DF508 mutation, both in heterozygote. Does the combination of these two mutations cause CF, or any other pathology? Thank you in advance.
- 22.06.2018
- Cystic Fibrosis Related Disorders
- I am 21 weeks pregnant. I was found to carry the DF508 CF mutation and my husband the c.220C>T (p.R74W). Does this combination cause mild or severe CF symptoms? Do you recommend an amniocentesis? We have two conflicting opinions. Thank you.
- 22.06.2018
- CF
- After an amniocentesis the CF mutations DF508 was found in the fetus. My wife does not carry the DF508 and was checked for 89% of CF mutations. I was tested and we await the results. Even if I am a carrier, what are the chances of the baby being a carrier or having CF? Thank you.
- 25.05.2018
- CF mutations
- The mother carries the mutation G542X in heterozygote status and the father the nucleotic change c.949G>C (p.Val317Leu) of the CFTR gene. The fetus, after an amniocentesis carries the G542X mutation from the mother and the p.Val317Leu mutation from the father. How severe will the CF be?
- 25.05.2018
- combination of DF508/R750Q
- I am 21 weeks pregnant in my first child and I was found to carry the DF508 mutation in heterozygote status. My husband was found to carry the R750Q mutation, also in heterozygote status. I would like to ask: 1. What are the chances of the fetus inheriting both genes? 2. What mild symptoms does this combination result in? 3. Is there a chance of the symptoms being severe? 4. What is the chance of sterility?
- 25.05.2018
- DF508 in heterozygote state
- After being tested for infertility for 75% (very small number of sperm cells) the DF508 mutation was found in heterozygote state. My wife will get tested for 99%. Must I get further testing? Apart for the infertility issue, are there any issues that I should know about?
- 25.05.2018
- cf prospects
- I am pregnant and carry the c. 2758G>T(p.Va1902Leu/V920L mutation of the CFTR gene, while my husband carries in heterozygote state the c.902A>GCp.Tyr301Cys/Y301c mutation in exon 7. What are the chances of the baby having CF? Thank you.
- 25.05.2018
- combination of DF508/NM_0004923
- My husband and I were found to be carriers of CF mutations. I have the DF508 mutation, and my husband carries the ΝΜ_0004923 mutation. What happens in this situation? What are the chances for our child to have CF? Thank you.
- 11.05.2018