Everything You Need To Know About Atypical Cystic Fibrosis

So far, there is limited research on atypical cystic fibrosis, primarily due to its rarity. While the diagnosis of classic cystic fibrosis is easier because of its evident symptoms and positive sweat test, the results for atypical forms are usually tricky, per a 2008 study published in the Journal of Cystic Fibrosis. In fact, sweat tests performed on atypical cystic fibrosis patients generally show borderline or normal results. Additionally, scientists found that diagnosis is only possible through follow-ups and examination of symptoms.

From the data available, it is clear that atypical cystic fibrosis commonly attacks just one organ at a time. According to a study from 2012, atypical cystic fibrosis may show symptoms in certain systems, such as respiratory, gastrointestinal, or endocrine. Some of the most common signs of atypical cystic fibrosis are recurring pneumonia, chronic sinusitis, nasal polyposis, diabetes, and nutritional deficiencies, among others. Fortunately, a 2020 research in Cureus reported that genetic testing could be viable and helpful in confirming the atypical cystic fibrosis diagnosis in clinical processes.

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