About the possibilities of APK “IMEDIS-EXPERT” in the case of arterial hypertension

AUTHORS : Kazantsev M.N.

RELEVANT UNIVERSITIES : Vladivostok, Russia

YEAR : 2021 | Category : Experience

Cystic fibrosis is rare, although the most common in Caucasiansan autosomal recessive life-limiting disorder. The pathology is caused by mutations or variations in the CFTR gene, which encodes a chlorine ion carrier channel. Since the CFTR protein is localized in the apical part of the membrane of epithelial cells lining the excretory ducts of the glands of external secretion (sweat, salivary, glands in the bronchi, pancreas, intestines, urogenital tract), multiple organ disorders associated with the secretion of thick secretions are noted in cystic fibrosis: sinusitis and chronic obstructive pulmonary disease (COPD), chronic pulmonary infections, pancreatitis, liver cirrhosis, colitis, male infertility.