Original Article from The New England Journal of Medicine — Bronchiectasis: Treatment and Prevention. Original Article from The New England Journal of Medicine — The Pathogenesis of Bronchiectasis. 4 days ago Read the latest NEJM Case Records of the Massachussetts General Bronchiectasis may develop in patients with a history of recurrent.
|Published (Last):||6 January 2007|
|PDF File Size:||18.32 Mb|
|ePub File Size:||8.69 Mb|
|Price:||Free* [*Free Regsitration Required]|
Show or Hide the password you are typing. This is the target of action of the drugs lumacaftor and tezacaftor.
We will not share your email with anyone. Bronchiectasis may develop in patients with a history of recurrent pneumonia, particularly those with chronic aspiration. There are close to recognized CFTR mutations, and each one confers a different degree of diminished chloride ion transport. Inthe qualifying mutations for the administration of ivacaftor were expanded to include DH. Primary ciliary dyskinesia can also cause left—right asymmetry.
Back to Social Login. Describe features of primary ciliary dyskinesia. Many lung infections can result in the development of bronchiectasis, including those caused by Mycobacterium tuberculosis and Bordetella pertussis. This type of mutation is the target of the drug ivacaftor, which restores partial ion transport.
Log in via Email. Mutations in CFTR disrupt sodium absorption, chloride secretion, and water transport, leading to the development bronchieftasis viscous mucus that adheres to the airway and impairs bacterial clearance. Request to Join has invited you to join this group.
Create your account Back to Social Login. A hypersensitivity response, known as allergic bdonchiectasis aspergillosis, may ensue, leading to a cycle of bronchial inflammation, mucoid impaction, and bronchial obstruction that results in bronchiectasis.
The CFTR protein forms a chloride channel that is critical to efficient mucus transport. Password must be at least 8 characters.
A Woman with Recurrent Sinusitis, Cough, and Bronchiectasis | NEJM Resident
Cystic fibrosis is a recessive genetic disease that is caused by mutations in both alleles of the CFTR gene, which encodes the cystic fibrosis transmembrane conductance regulator CFTR.
The primary defect that is caused by the Phedel mutation is that the CFTR protein is synthesized but misfolded, which keeps it from reaching the cell surface. The DH mutation is considered to be a partial-function mutation that results in diminished ion transport. Primary ciliary dyskinesia is a congenital, autosomal recessive disorder that is characterized by immotile or dyskinetic cilia.
What are some of the causes of bronchiectasis? In addition to impaired airway clearance, fertility problems can arise in males as a result of impaired spermatozoa motility and in females as a result of impaired ciliary function in the oviduct.
A Woman with Recurrent Sinusitis, Cough, and Bronchiectasis
Therefore, nodal ciliary dysfunction can produce dextrocardia, situs inversus totalis, and situs ambiguus. Bronchiectasis is characterized by irreversible damage of the airways that results in dilatation. With the administration of these treatments at cystic fibrosis—specific treatment centers, median survival has increased from In some people, inhalation of Aspergillus fumigatus provokes a brisk allergic response that is characterized by eosinophilia and a high level of IgE antibodies.
Patients with immunodeficiency syndromes are at high risk for the development of bronchiectasis.