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Information × Registration Number 0211U008866, 0107U011954 , R & D reports Title The analyses of medical-genetic counseling effectiveness in families with children, carrying socially important congenital anomalies. popup.stage_title Head Hnateyko Oleh, Registration Date 16-11-2011 Organization Scientific-research institute of Hereditary pathology popup.description2 During 2002-2007 363 cases of model congenital anomalies among 154421 newborn in Lviv region registered (frequency equals 23.5 per 10000). In 2007 there were 58 cases of model birth defects registered among 27454 newborn (frequency equals 21.1 per 10000). The frequencies of stillbirths, placenta pathology, pregnancy complications in the second half, preterm delivery, low Apgar estimation (under 8), acute infectious diseases 3 months earlier and during pregnancy in the examined group of women were significantly higher, than in controls (Р<0,05). Among birth defects of urinal system in small children the anomalies, associated with widening of urinal tracts, occurred more frequently (55.2 %). The frequency of anomalies of kidney's number or position was at the level of 37.2 %. Clinical studies in Lviv district showed significantly increased level of frequency of acute lymphoblast leucosis in children, who's mothers worked as seamstresses before and during the pregnancy. The medical-genetic counseling in such families helps to predict birth defects of heart, skeleton, reproductive system in 1 degree relatives. Product Description popup.authors Гельнер Надія Володимирівна Геник-Березовська Софія Олександрівна Гнатейко Олег Зіновійович Грузинцева Наталія Анатоліївна Зборовська Наталія Володимирівна Кіцера Наталія Іванівна Косминіна Неля Станіславівна Лук'яненко Наталія Сергіївна Лучак Марта Володимирівна Прокопчук Наталія Миколаївна Чайковська Галина Степанівна Школьник Михайло Борисович Шуварська Віра Іванівна popup.nrat_date 2020-04-02 Close
R & D report
Head: Hnateyko Oleh. The analyses of medical-genetic counseling effectiveness in families with children, carrying socially important congenital anomalies.. (popup.stage: ). Scientific-research institute of Hereditary pathology. № 0211U008866
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Updated: 2026-03-27