There are no 'Side Effects', just things that 'come with the package'.
You can suffer breathlessness, bowel problems and probalmes with liver and kidneys. There are other things too, but at age 13, that's all I've really had so far.
Karyotyping looks at the complete set of chromosomes. It can detect large-scale abnormalities, such as missing/extra chromosomes or whether large pieces of chromosomes have been rearranged. It cannot detect any of the many, many genetic disorders which are caused by a single gene, several genes or gene interactions. Examples of these would be cystic fibrosis, sickle-cell disease and dwarfism.
The CFTR (cystic fibrosis transmembrane conductance regulator) gene contains 27 exons. These exons encode the protein responsible for regulating chloride ions across epithelial cell membranes, and mutations in this gene are associated with cystic fibrosis.
The life expectancy of individuals with cystic fibrosis has significantly improved over the years due to advancements in treatments and therapies. However, it is still considered a life-shortening disease, with most individuals living into their 30s and 40s. With proper management and care, many people with cystic fibrosis can lead fulfilling lives.
Autosomal disorders generally have a greater impact on a person's health compared to sex chromosome disorders. This is because autosomal chromosomes carry a wider range of genes that influence various bodily functions and traits, and many autosomal disorders can lead to severe developmental and health issues, such as Down syndrome or cystic fibrosis. In contrast, sex chromosome disorders, like Turner syndrome or Klinefelter syndrome, often have more specific effects and may not be as universally debilitating.
Chromosome therapy is a theoretical approach that involves altering chromosomes, which contain an individual's genetic information, to treat genetic disorders or diseases. This field is still largely experimental and faces many ethical and technical challenges. It is exploring the potential to correct genetic abnormalities at the chromosomal level.
Cystic fibrosis is widely recognized as a lung disease, but it is actually a disease that affects many parts of the body. So yes. it can:) hope this is helpful
There is no cystic fibrosis centre in pakistan But Agha khan hospital karachi is best to diagnoseand treat cystic fibrosis patients .Almost all the medications of cystic fibrosis are available in Pakistan.
The person who has Cystic Fibrosis has it for life.
cystic fibrosis
Unfortunately, cystic fibrosis cannot be cured by prayer. If it could be cured by prayer, the disease would have disappeared a long time ago, because there are a great many people praying all the time. We have a great abundance of prayer, in this world. But we still have cystic fibrosis.
1 in every 8000
Sickle cell anemia and cystic fibrosis are carried on autosomes (chromosomes other than the sex chromosomes). Probably too many to list . . Right now, off the top of my head, I can think of Down's Syndrome (21st chromosome) and the "cri du chat" (5th chromosome) . . .
Karyotyping looks at the complete set of chromosomes. It can detect large-scale abnormalities, such as missing/extra chromosomes or whether large pieces of chromosomes have been rearranged. It cannot detect any of the many, many genetic disorders which are caused by a single gene, several genes or gene interactions. Examples of these would be cystic fibrosis, sickle-cell disease and dwarfism.
go to www.cdc/gov.com :D hope i helped
Cystic fibrosis (CF) is a rare genetic disorder, and its prevalence can vary by region. In Mississippi, it is estimated that there are approximately 100 to 200 individuals living with cystic fibrosis. The exact number can fluctuate due to factors such as population size and the availability of medical resources. For the most accurate and up-to-date information, it is advisable to consult local health departments or CF registries.
The CFTR (cystic fibrosis transmembrane conductance regulator) gene contains 27 exons. These exons encode the protein responsible for regulating chloride ions across epithelial cell membranes, and mutations in this gene are associated with cystic fibrosis.
Deaths from Cystic Fibrosis: 485 deaths (NHLBI 1999)Death rate extrapolations for USA for Cystic Fibrosis: 484 per year, 40 per month, 9 per week, 1 per day, 0 per hour, 0 per minute, 0 per second. Note: this extrapolation calculation uses the deaths statistic: 485 deaths (NHLBI 1999)45 people died from cystic fibrosis in Australia 2000 (Australia's Health 2004, AIHW)Source(s):RRT