DIAGNOSTIC PROBLEMS OF MUCOVISCIDOSIS AND WAYS OF SOLUTION IN RUSSIA
https://doi.org/10.15690/pf.v11i6.1211
Abstract
Mucoviscidosis is a monogenic autosomal recessive caused by the CFTR gene mutations and characterized by pronounced genetic heterogeneity and clinical polymorphism, which emphasizes the need in comprehensive diagnosis and molecular-genetic verification of the final diagnosis. Quality and duration of a mucoviscidosis patient depend on early diagnosis and timely adequate therapy. The article presents mucoviscidosis diagnostic methods and protocols and capabilities of the modern molecular-genetic pathological diagnosis; a review of DNA diagnostic sets has been performed. As sets of some of the genes typical to the Russian population have not been registered in the Russian Federation, mutations in 20% of the patients cannot be specified. In order to solve this problem it is necessary to develop DNA diagnostic sets specific for the Russian Federation, ensure genetic diagnosis of the disease, including sequencing methods at the expense of the federal budget, increase the amount of information and improve quality of teaching this discipline to students of medial universities and at postgraduate courses for appropriate specialists.
About the Authors
A. A. BaranovRussian Federation
N. I. Kapranov
Russian Federation
N. Yu. Kashirskaya
Russian Federation
L. S. Namazova-Baranova
Russian Federation
V. D. Sherman
Russian Federation
O. I. Simonova
Russian Federation
A. Yu. Tomilova
Russian Federation
K. V. Sevost'yanov
Russian Federation
A. M. Pushkov
Russian Federation
A. L. Vladykin
Russian Federation
N. V. Shatokhin
Russian Federation
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Review
For citations:
Baranov A.A., Kapranov N.I., Kashirskaya N.Yu., Namazova-Baranova L.S., Sherman V.D., Simonova O.I., Tomilova A.Yu., Sevost'yanov K.V., Pushkov A.M., Vladykin A.L., Shatokhin N.V. DIAGNOSTIC PROBLEMS OF MUCOVISCIDOSIS AND WAYS OF SOLUTION IN RUSSIA. Pediatric pharmacology. 2014;11(6):16-23. (In Russ.) https://doi.org/10.15690/pf.v11i6.1211