Faculty Opinions recommendation of One-cell zygote transfer from diabetic to nondiabetic mouse results in congenital malformations and growth retardation in offspring.

Author(s):  
Tim Schedl
2016 ◽  
Vol 21 (32) ◽  
pp. 57-62
Author(s):  
Каркусова ◽  
Alla Karkusova ◽  
Бураева ◽  
Zarina Buraeva

Perinatal pathology, including congenital malformations of the fetus, is a serious problem of today’s society. The purpose of this study was to identify the significance of oligohydramnios in the diagnosis of congenital diseases in children. The study involved 140 pregnant women aged 18 to 42 years. It was found that while simultaneous revealing of oligohydramnios, fetal growth retardation, abnormal cardiotocography types, hemodynamic disturbances in the utero-placental blood flow risk of having children with congenital malformations is increased by 1.5 times. Thus, a more detailed search for the ultrasonic markers of congenital diseases, timely consulting of families in medical genetics facilities while oligohydramnios allows to prevent severe perinatal outcomes.


PEDIATRICS ◽  
1988 ◽  
Vol 82 (1) ◽  
pp. 83-90 ◽  
Author(s):  
Muin J. Khoury ◽  
J. David Erickson ◽  
José F. Cordero ◽  
Brian J. McCarthy

The relationship between congenital malformations and intrauterine growth retardation was investigated using data from the population-based Metropolitan Atlanta Congenital Defects Program. Between 1970 and 1984, the system ascertained 13,074 infants with major structural malformations diagnosed in the first year of life and born to metropolitan Atlanta residents. These infants were classified as having intrautenine growth retardation if their birth weight was below the race-, sex-, and gestational age-specific tenth percentile limits for all Atlanta births. Overall, the frequency of intrauterine growth retardation among malformed infants was 22.3% (relative risk 2.6). Of 48 defect categories evaluated, 46 were associated with excess intrauterine growth retardation, most notably chromosomal anomalies (eg, 83.7% for infants with trisomy 18, relative risk 46) and anencephaly (73.3%, relative risk 25). Only a few isolated defects (such as isolated polydactyly, pylonic stenosis, and congenital hip dislocation) were not associated with excess intrauterine growth retardation. Among infants with multiple malformations, the frequency of intrauterine growth retardation increased markedly with increasing number of defects—from 20% for infants with two defects to 60% for infants with nine or more defects. The relationship between malformations and intrauterine growth retardation can be explained by one or more of three mechanisms: (1) intrauterine growth retardation can be a secondary disturbance to the presence of malformations; (2) intrauterine growth retardation can predispose the fetus to malformations; and (3) intrauterine growth retardation can coexist with malformations because of common etiologic factors. Because the risk of a major defect diagnosed in the first year increases from 3.3% for infants without intrauterine growth retardation to 8.0% for infants with intrauterine growth retardation, the presence of intrauterine growth retardation may help in the prenatal and neonatal detection of congenital malformations.


PEDIATRICS ◽  
1989 ◽  
Vol 84 (4) ◽  
pp. A84-A84
Author(s):  
Student

LWB is part of the complex interactions of such factors as prenatal growth retardation, prematurity, complications of labor and delivery, congenital malformations, and adverse prenatal and postnatal social and psychological influences. These factors cannot be separated easily to show separate impacts.


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