A survey of primary infantile and juvenile pneumonia.
نویسنده
چکیده
Statistical review The material for review was collected from the records of three Dublin Hospitals for the years 1937 to 1939. All patients dying within twentyfour hours of admission, or in whom signs of improvement had set in before starting treatment, were excluded. The cases were clinically divided into the two groups of lobar and atypical pneumonia. The former showed clinical evidence of lobar consolidation, the latter consolidation of an irregular patchy nature. Eight hundred and ninety-five cases were studied. Table 1 shows the age group distribution, and table 2 the combined fatality rates for the three years studied. TABLE 1
منابع مشابه
The effect of down-regulation of CCL5 on lipopolysaccharide-induced WI-38 fibroblast injury: a potential role for infantile pneumonia
Objective(s): Aberrant expression of CCL5 has been found in several kinds of inflammatory diseases, and the roles of CCL5 in these diseases have also been reported. However, the role of CCL5 in infantile pneumonia is still unclear. Thus, the function and acting mechanism of CCL5 in the in vitro model of infantile pneumonia were researched in this study. Materials and Methods: Human fetal lung f...
متن کاملStudy on Mycoplasmal pneumonia at the Ziaran abattoir
I n a survey of pneumonia due to Mycoplasma 282 out of 12168 ovine and caprine lung condemnation were collected (2.32%). Mycoplasma spp. has been isolated from pneumonic cases in 4 sheep and 2 goats. PCR studies were confirmed the genus of Mycoplasma although attempting for identification of strains M. mycoides, M. capricolum/caprine pleuropneumonia and M. arginin were in failure. The lesions...
متن کاملClinical Relevance of Faecal Calprotectin Level in Infantile Colic: A Cross-sectional Survey
Background: There is limited knowledge on the potential applicability of fecal calprotectin (f-CP) as an inflammatory screening parameter in infantile colic (IC). This study aimed to evaluate f-CP in neonates with IC as a useful diagnostic indicator regarding this condition. Methods: The present study was conducted on 100 cases, including 50 newborns with IC and 50 non-colicky neonates. The dia...
متن کاملAlsin Related Disorders: Literature Review and Case Study with Novel Mutations
Mutations in the ALS2 gene cause three distinct disorders: infantile ascending hereditary spastic paraplegia, juvenile primary lateral sclerosis, and autosomal recessive juvenile amyotrophic lateral sclerosis. We present a review of the literature and the case of a 16-year-old boy who is, to the best of our knowledge, the first Portuguese case with infantile ascending hereditary spastic paraple...
متن کاملScreening of CYP1B1 Arg368His as predominant mutation in North Indian primary open angle glaucoma and juvenile onset glaucoma patients
In India, mutations in Cytochrome P450 (CYP1B1) are a predominant cause of not only primary congenital glaucoma (PCG) but also involved in primary open angle glaucoma (POAG) and juvenile onset glaucoma (JOAG). After ethical clearance, 100 POAG patients, 30 primary angle closure glaucoma (PACG) patients and 130 ethnically matched controls were recruited in this study. Genomic DNA was is...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Archives of disease in childhood
دوره 16 86 شماره
صفحات -
تاریخ انتشار 1941