Spontaneous
Resolution of Prenatally Diagnosed Pleural Effusion: A Case Report by Slagjana
Simeonova Krstevska* in Open Access Journal
of Biomedical Science (OAJBS)
Mucocidosis
(cystic fibrosis) is the most common autosomal recessive inherited multisystem
disease with a very deadly and dangerous outcome due to mutations and
sequential mutations in the gene regulating the transmission of cystic fibrosis
membrane (CFTR) leading to the chloride channel. And the CFTR protein becomes
unhealthy and destructive [1,2]. As a result of the collection and collection
of mucus that is not sufficiently hydrated and hydrophilic, it affects various
basic organs, mainly lungs, and airways, pancreas, liver, bile ducts and
intestines. This leads to inflammation and infection, fibrosis, and gradual
tissue destruction [3-5]. Respiratory failure and subsequent problems have been
cited as one of the leading causes of death. However, more than 30 years of
molecular description A major defect in CFTR causes CF, a remarkable success in
the long-term prognosis of people with CF. This breakthrough is very active in
the spirit of collaboration and networking of the CF research community, and
internationally, with the creation of a multidisciplinary clinical CF team that
implements evidence in various aspects of standard care with the CF patient has
been obtained. Rath et al. [5]. In their study found that several bacteria and
fungi that cause organisms are also known as urinary tract infections (UTIs)
that may occur in more than 50% of the population and are more common in women
[5-8].
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