Fibrosis leads to the thickening and stiffening of tissues, which decreases the compliance of affected organs, such as the lungs or heart. This reduced compliance means that the organ cannot expand or contract as easily, resulting in impaired function. In the lungs, for instance, fibrosis can hinder effective gas exchange, while in the heart, it can affect the heart's ability to fill with blood properly. Overall, fibrosis disrupts normal physiological dynamics and can lead to significant health issues.
yes, everyone who has cystic fibrosis has had it from birth therefore they have it when they are children.
it kills you
Cystic Fibrosis
Cystic fibrosis happens due to mutations in a gene called CFTR and an abnormal behavior impairs homeostasis inside the cell. Cyst
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
Lung compliance is determined by the elasticity of the lung tissue and the surface tension of the alveoli. Compliance decreases with conditions that stiffen the lung tissue, such as fibrosis, or increase surface tension, such as pulmonary edema. Compliance also decreases with aging and certain diseases like chronic obstructive pulmonary disease (COPD).
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No, cystic fibrosis affects males and females equally. It is an inherited genetic disorder caused by mutations in the CFTR gene, which can be passed down from each parent who carries a mutated gene.
Five that come to mind: lung cancer, cystic fibrosis, asthma, emphysema, tuberculosis
Yes, the Cystic Fibrosis Foundation does support research that may involve animal testing as part of the development of new therapies for cystic fibrosis. This research aims to better understand the disease and evaluate the efficacy and safety of potential treatments. The foundation prioritizes ethical research practices and works to ensure that any animal testing is conducted in compliance with regulations and standards.
Static compliance decreases due to factors like pulmonary fibrosis, lung tissue scarring, or poor surfactant function which results in reduced ability of the lungs to stretch and expand during inhalation, leading to decreased lung capacity and restricted airflow.
I was told Irish and Australian nationalities.