从零开始:婴儿期幽门狭窄病因的原发性高酸性理论

Q4 Medicine Journal of Neonatal Surgery Pub Date : 2022-01-14 DOI:10.47338/jns.v11.1004
I. Rogers
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引用次数: 0

摘要

最初描述婴儿幽门狭窄(PS)的人的早期观察结果被用作遗传原发性高酸度病因理论发展的背景。这些早期的真相,通过现代技术并不复杂,已经成为发病机制的跳板。高酸度、男性优势、家族史、自我治疗、食欲增强和对时间敏感的表现都是早期先驱所熟知的。任何一种发病机制都必须解释所有这些临床特征。继承的原发性高酸度理论做到了这一点,是对这些早期先驱建立的所有临床特征的可信解释。有证据支持胃泌素和胃酸之间负反馈的成熟延迟。这样的现象进一步支持了初级超酸性理论。
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Starting from scratch: The primary hyperacidity theory of the cause of pyloric stenosis of infancy
The early observations of those who first described babies with pyloric stenosis (PS) are used as a backdrop for the development of the Inherited Primary Hyperacidity theory of cause. Those early truths, uncomplicated by modern technology, have acted as a springboard for pathogenesis. Hyperacidity, male predominance, family history, self-cure, enhanced appetite, and time-sensitive presentation were all well known to the early pioneers. Any system of pathogenesis must explain all these clinical features. The Inherited Primary Hyperacidity theory does this and is a credible explanation for all the clinical features established by these early pioneers. The evidence which supports a delay in maturation of the negative feedback between gastrin and gastric acidity is presented. Such a phenomenon further supports the Primary Hyperacidity theory.
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来源期刊
Journal of Neonatal Surgery
Journal of Neonatal Surgery Medicine-Surgery
CiteScore
0.30
自引率
0.00%
发文量
29
审稿时长
6 weeks
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