Department of Pneumonology, University of Vienna, Universitätsring 1, 1010 Wien, Austria
 Mini Review   
								
																Tuberculosis and Cystic Fibrosis: Understanding the Intersection of Two Respiratory Challenges 
																Author(s): Aleksandra Mikos*             
								
																
						 Tuberculosis (TB) and Cystic Fibrosis (CF) are two distinct yet significant respiratory conditions that affect millions of people worldwide. While they
  differ in their origins, symptoms and treatments, the intersection of TB and CF poses unique challenges for individuals who face both conditions
  simultaneously. Tuberculosis (TB) is a bacterial infection caused by Mycobacterium tuberculosis, a pathogen that primarily affects the lungs but
  can potentially target other organs in the body. TB has been a significant public health concern for centuries and continues to impact millions of
  people worldwide. To better understand this infectious disease, let's delve into its causes, transmission, symptoms, diagnosis and treatment. Cystic
  Fibrosis, on the other hand, is a genetic disorder characterized by the production of thick and sticky mucus that clogs the airways and various
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																DOI:
								10.37421/2472-1247.2023.9.272