Congenital pyloric stenosis; an investigation of 578 cases.
نویسندگان
چکیده
In the case of pyloric stenosis, the collection of this information now raises no insuperable difficulty, and if knowledge (of such matters as the association of the malformation with maternal age and birth rank) is still incomplete, it is because inquiries have usually been based on hospital births for which the population of related births is unknown. In the present investigation we have attempted to overcome this difficulty by the following methods: (1) A series of Birmingham children with pyloric stenosis has been assembled by examination of the records of all Birmingham hospitals which admit children, for the 10-year period 1940-49. t (It was, of course, necessary to exclude children whose homes were not in Birmingham.) The series can be regarded as complete in so far as
منابع مشابه
First Report of A Unique Presentation of Hypertrophic Pyloric Stenosis Following Type I Esophageal Atresia; A Case Report
Combination of congenital esophageal atresia and subsequent hypertrophic pyloric stenosis is a rare condition which occurs in early infancy. The underlying etiology and pathophysiology of this association still remains unclear. In this paper we report a unique case of hypertrophic pyloric stenosis, for the first time, which occurred in an infant who underwent surgery for type I esophag...
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Based on evidence from two collected and treated clinical observations of hypertrophic pyloric stenosis in children of 5 and 12 months of age, the authors give their point of view on the unresolved issue of the etiology of hypertrophic pyloric stenosis. They emphasize that there are more and more factors to prove this is an acquired condition.
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ورودعنوان ژورنال:
- British journal of social medicine
دوره 5 3 شماره
صفحات -
تاریخ انتشار 1951