ECHO 9 VIRUS INFECTION AND CONGENITAL ABNORMALITIES: A NEGATIVE REPORT

PEDIATRICS ◽  
1962 ◽  
Vol 29 (2) ◽  
pp. 261-269
Author(s):  
Herman Kleinman ◽  
James T. Prince ◽  
Wayne E. Mathey ◽  
Abraham B. Rosenfleld ◽  
Jacob E. Bearman ◽  
...  

Approximately 200,000 residents of Hennepin and Ramsey counties in Minnesota developed an aseptic meningitis syndrome during the summer and fall of 1957. One fourth of the patients had a maculopapular rash very similar to that of rubella. The etiologic agent was found to be ECHO virus type 9. This epidemic provided an opportunity to determine whether infection with this virus during the first trimester of pregnancy could be related to the appearance of congenital defects such as occurs in rubella. From March 3 through June 13, 1958, 10,109 liveborn infants and 105 stillborn infants were delivered in the 12 Minneapolis and 10 St. Paul hospitals serving these two counties. All mothers had been exposed to the 1957 epidemic. Public health nurses interviewed 9,990 mothers in the hospitals within a few days after birth for detailed histories of infection during pregnancy. On the basis of these interviews it was judged that 6.5% of the mothers had historic evidence of an ECHO 9 infection during pregnancy. Serologic evidence of ECHO 9 infection in the recent past was present in 19% of 853 antibody titrations carried out on cord blood specimens from abnormals and normals (controls). To discover anomalies not recognized at birth, a follow-up was carried out 11 to 12 months later by the public health nurses by telephone interviews of some 9,600 mothers. There were 356 major and minor congenital anomalies recognized during the first year of life. An additional 63 hernias were diagnosed during the first year for a total of 419 anomalies found in 10,109 live births in the study. This rate of 41.4 total anomalies per 1,000 live births, or 4.1%, is well within the rates reported by other authors. A total of 39.6% of the anomalies were diagnosed at birth and 60.4% during the first year of life. Of the anomalies, 61% occurred in males and 39% in females; 1.5% of the infants had major abnormalities and 0.74% died as a result of these anomalies during their first year of life. There were 105 stillbirths recorded, or 10.4 per 1,000 live births. This compares with a rate of 13.6 for Hennepin and Ramsey counties for the year. Among the stillbirths, 11.4% died from congenital anomalies, in comparison with 10.95% statewide for the year. A statistical analysis of the findings which compares the ECHO 9 antibody titer distributions in the cord blood of the normal and the abnormal infants does not justify the conclusion that ECHO 9 infection in the mother increases the incidence of congenital anomalies in the offspring. The only exception to this generalization is in the case of skin abnormalities, where there is a statistical suggestion of association.

2014 ◽  
Vol 33 (4) ◽  
pp. 199-203 ◽  
Author(s):  
Angela Koerner

According to multiple researchers and studies, congenital heart disease (CHD) occurs in approximately 4.8–12.0 of 1,000 live births in the general population, and 2.4 per 1,000 cases are serious enough to require surgery or cardiac catheterization in the first year of life.1 Historically, it has been assumed that the earlier the gestational age with CHD, the poorer the outcome; however, with continued improvements in neonatal care, this hypothesis should be looked at more closely. This case illustrates the challenges associated with prematurity, complex cardiac defects, intraventricular hemorrhage (IVH), and other congenital anomalies that increase the risk of infection and/or surgical intervention. It will discuss the hospital course of a twin, born at 27 weeks gestation, who was found to have all of these diagnoses, yet, despite the complexity of his case, he had a predominantly uncomplicated hospital course.


2009 ◽  
Vol 20 (3) ◽  
pp. 227-233 ◽  
Author(s):  
Hiromi Tadaki ◽  
Hirokazu Arakawa ◽  
Mikio Sugiyama ◽  
Kiyoshi Ozawa ◽  
Takahisa Mizuno ◽  
...  

Thorax ◽  
2018 ◽  
Vol 74 (2) ◽  
pp. 200-202 ◽  
Author(s):  
Hooman Mirzakhani ◽  
Amal A Al-Garawi ◽  
Vincent J Carey ◽  
Weiliang Qiu ◽  
Augusto A Litonjua ◽  
...  

Cord blood 25-hydroxyvitamin D (25OHD) has been reported in association with risk of early life recurrent wheeze. In a subset of infants who participated in the Vitamin D Antenatal Asthma Reduction Trial, we demonstrated that higher cord blood 25OHD at birth (>31 ng/mL) was associated with a reduced risk of recurrent wheeze in the first year of life. We then identified a module of co-expressed genes associated with cord blood 25OHD levels >31 ng/mL. Genes in this module are involved in biological and immune pathways related to development and progression of asthma pathogenesis including the Notch1 and transforming growth factor-beta signalling pathways.


2016 ◽  
Vol 3 (3) ◽  
pp. 202-203
Author(s):  
Craig Hansen ◽  
Susan E Adrade ◽  
Heather Freiman ◽  
Sascha Dublin ◽  
Katie Haffenreffer ◽  
...  

2014 ◽  
Vol 5 (3) ◽  
pp. 214-218 ◽  
Author(s):  
J. L. Kaar ◽  
J. T. Brinton ◽  
T. Crume ◽  
R. F. Hamman ◽  
D. H. Glueck ◽  
...  

Objective: To examine the association of cord blood leptin with body mass index (BMI) growth velocity from birth to 12 months of age among infants exposed and not exposed to over-nutrition in utero (defined as maternal overweight/obesity or presence of gestational diabetes). Methods: 185 infants enrolled in the Exploring Perinatal Outcomes among Children study (76 exposed and 109 not exposed) had leptin and insulin measured in cord blood. Longitudinal weight and length measures in the first 12 months of life (average 4 per participant) obtained from medical records were used to compute BMI growth rates. Mixed models were used to examine associations of cord blood leptin with growth. Results: Compared with unexposed infants, those exposed had significantly higher cord blood insulin (8.64 v. 6.97 uU/ml, P<0.01) and leptin levels (8.89 v. 5.92 ng/ml, P=0.05) as well as increased birth weights (3438.04 v. 3306.89 g, P=0.04). There was an inverse relationship between cord leptin levels and BMI growth from birth to 12 months of age (P=0.005); however, exposure to over-nutrition in utero did not significantly modify this association (P=0.59). Conclusion: We provide support of a possible operational feedback mechanism by which lower cord blood leptin levels are associated with faster infant growth in the first year of life. Our data do not tend to support the hypothesis that this mechanism is altered in infants exposed to over-nutrition in utero; however our sample is too small to provide sufficient evidence. Larger epidemiological studies are needed to elucidate the mechanisms responsible for increased propensity for obesity in exposed offspring.


2017 ◽  
Vol 23 (1) ◽  
pp. 96-102 ◽  
Author(s):  
Annalisa Ruggeri ◽  
Fernanda Volt ◽  
Franco Locatelli ◽  
Gerard Michel ◽  
Cristina Diaz de Heredia ◽  
...  

2020 ◽  
Vol 14 (4) ◽  
pp. 32-37
Author(s):  
R. G. Gamirova ◽  
N. G. Lyukshina ◽  
R. R. Gamirova ◽  
M. E. Farnosova

Kleefstra syndrome is a rare autosomal dominant genetic disorder caused by haploinsufficiency of the EHMT1 (Euchromatic Histone MethylTransferase 1). Patients with Kleefstra syndrome have following most common symptoms: moderate or severe intellectual deficiency, absence of speech, significant diffuse muscular hypotonia, micro-brachycephaly, congenital defects of heart, kidneys, genitourinary tract and recognizable dysmorphic features of face. The article presents 2 similar clinical cases of Kleefstra syndrome in combination with epilepsy. Both patients, along with a typical clinical picture of the underlying disease, have serial epileptic spasms with an onset after first year of life, modified hypsarrhythmia with tendency to synchronization on the electroencephalogram, pharmacoresistant epilepsy. This indicates that Kleefstra syndrome can include epilepsy as one of symptoms of the disease.


2020 ◽  
pp. 24-32
Author(s):  
R.V. Marushko ◽  
◽  
О.О. Dudina ◽  
T.L. Marushko ◽  
◽  
...  

Ukraine entered the 21st century with one of the worst vital signs in Europe and the burden of many socio-economic and demographic problems. Adverse quantitative and especially qualitative indicators of population reproduction have become stable. Therefore, the most important medical and social task and one of the main activities of the Ministry of Health of Ukraine is the formation and maintenance of public health. The defining stage in the formation of human health is the first year of life. Purpose — to study the state and trends of changes in the main indicators of the health of children in the first year of life for the period 2000–2019. Materials and methods. A retrospective analysis of the incidence of children in the first year of life, infant mortality, over the past 20 years in the context of individual pathological conditions is carried out. The information base of the study was the data of state and industry statistics for 2000–2019. Methods of a systematic approach, statistical data processing, epidemiological analysis of graphic images were used. Results. The study revealed that the unfavorable demographic situation in Ukraine is accompanied by an unsatisfactory state of the main predictors of a healthy start in the life of infants, the formation and maintenance of their health. Over the past two decades, there has been a high level with a negative trend of diseases of the reproductive system of women, a high frequency of the combination of pregnancy and extragenital diseases remains. There is a negative trend towards an increase in the generalized objective criterion of the health of the generation, which is born and the socio-economic well-being of the population — the frequency of premature, low birth weight, incl. With very low birth weight. Only thanks to the introduction of modern medical organizational technologies with proven efficiency in the activities of the maternal and child health service was it possible to achieve a decrease in the incidence of newborns from 280.8 per 1000 live births in 2000 up to 172.14 in 2019. At the same time, the increase in the incidence of newborns with diseases that have a direct impact on the development of chronic and disabling diseases at all stages of life is of concern — congenital pneumonia, neonatal sepsis, other disorders of the cerebral status of the newborn, neonatal jaundice. According to the assessment of the dynamics of the general morbidity of children in the first year of life, its level is still high, with a positive trend — 2018.8 per 1000 children who reached 1 year in 2000 and 1393.1 in 2019, the growth rate is -30.9% with a traditionally leading position in the level and structure of the incidence of respiratory diseases — 810.2 per 1000 children who have reached one year of life and 58.15%, certain conditions occurring in perinatal period — 126.7 ‰ and 9.06%, diseases of the skin and subcutaneous tissue — 63.9‰ and 4.59%, diseases of the blood and hematopoietic organs and certain disorders involving the immune mechanism — 63.0‰ and 4.52%. Conclusions. The positive dynamics of morbidity in children of the first year of life is confirmed by a decrease in infant mortality from its maximum level of 11.9 per 1000 live births in 2000 up to 7.0 in 2019, the growth rate is -41.2% due to all its components with a more intensive reduction in postneonatal mortality from 5.28‰ to 2.57‰, the growth rate is -51.3% against the background of an increase in the concentration of mortality in the neonatal period from 55.9% to 64.5%, respectively. No conflict of interest was declared by the authors. Key words: newborns, children of the first year of life, low birthweight newborns, morbidity, infant mortality.


2021 ◽  
Vol 19 (1) ◽  
pp. 62-65
Author(s):  
Sahisnuta Basnet ◽  
Eva Gauchan ◽  
Junu Shrestha ◽  
Jyoti Jha

Background: The study is aimed at highlighting the pattern of congenital defect in a tertiary care hospital. Congenital anomalies are recognized as a growing cause of neonatal morbidity and mortality in developing countries and a major cause of distress to parents.Methods: This was a prospective descriptive study conducted between September 2019 and August 2020 with the objective to determine the types of congenital anomalies among live born neonates at Manipal Teaching Hospital (MTH), Pokhara and to determine their immediate outcome. Neonatal and maternal characteristics were noted.Results: Twenty four out of 2515 live births had congenital anomalies during the study period, giving an incidence rate of 9.42 congenital anomalies per 1000 live birth per year. Single system involvement was seen in 79.2 % cases, remaining 5 (20.8%) neonates had involvement of more than one system; 54.2% of these newborns were discharged, 33.3% expired, 8.3% left against medical advice and 4.2% were referred out.Conclusions: This study highlights the importance of clinical examination of neonates to detect anomalies in our setting. Keywords: Congenital anomalies; incidence; newborn


Sign in / Sign up

Export Citation Format

Share Document