22q11.2 DELETION SYNDROME: ALGORITHM FOR THE EARLY DIAGNOSIS AND TREATMENT
https://doi.org/10.15690/vsp.v16i5.1803
Abstract
Chromosomal diseases, in particular microdeletions, determine the child's condition as well as the prognosis for a disease even at birth. With timely identified chromosomal abnormalities, we can diagnose not only obvious but also hidden disorders in the organs and their systems and timely correct the child's treatment at an early age. The algorithm for diagnosis of chromosomal abnormalities in children is an important component of a modern pediatric practice. It allows to increase the effectiveness of chromosomal pathology treatment.
About the Authors
Leyla S. Namazova-BaranovaRussian Federation
Disclosure of interest: receiving research grants from pharmaceutical companies Pierre Fabre, Genzyme Europe B.V., AstraZeneca Pharmaceuticals, Gilead / PRA Pharmaceutical Research Associates CIS, Teva Branded Pharmaceutical Products R&D, Inc / PPD Development (Smolensk), Stallergenes S.A. / Quintiles GeismbH (Austria)
Olga V. Ginter
Russian Federation
Tatyana A. Polunina
Russian Federation
Irina V. Davydova
Russian Federation
Disclosure of interest: cooperates with Abbvie
Kirill V. Savostyanov
Russian Federation
Alexandr A. Pushkov
Russian Federation
Natalya V. Jourkova
Russian Federation
Tatyana Y. Mospan
Russian Federation
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Review
For citations:
Namazova-Baranova L.S., Ginter O.V., Polunina T.A., Davydova I.V., Savostyanov K.V., Pushkov A.A., Jourkova N.V., Mospan T.Y. 22q11.2 DELETION SYNDROME: ALGORITHM FOR THE EARLY DIAGNOSIS AND TREATMENT. Current Pediatrics. 2017;16(5):392-398. (In Russ.) https://doi.org/10.15690/vsp.v16i5.1803