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Study of the Occurance of Labio-Palatine Cleft Embryogenic Disorders of the Stomatognated System by Using Lots of Wistar Rats Females

机译:用Wistar大鼠女性研究气囊腭腭胚胚胎源性疾病的研究

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摘要

Labio-maxilo-palatine clefts are embryogenesis disorders of the stomatognathic system that occur due to the action of genetic or non-genetic factors in weeks 5-6 of intrauterine life. The clefts are part of the group of congenital malformations of the face. They appear from birth as a slit in the upper lip, hard palate and/or soft palate. Labio-maxilo-palatine cleafts are a current medical problem, especially regarding surgical recovery; they are congenital malformations of the face characterized by the absence of substance in the upper lip and/or in the palatine vault caused by the lack of fusion of labial and / or palatine buds during embryonic development Simple labial cleft concerns only the lip, unlike the complete labial cleft which affects also the alveolar maxillary arch. In the case of this malformation, more serious than labial cleft, the cleft also affects the bone structures (the alveolar maxillary arche, the buccal palate) so that the oral cavity communicates with the nasal cavity and prevents sucking in infants. An early surgical recovery restores the integrity of anatomical structures, reestablishes disturbed functions, creates favorable conditions for speech education and social adaptation of the child according to age. The procedure is applied prior to the primary suture of the lip and of the anterior palate in order to minimize the dislocation of the segments of the maxillary arch. The correction of the malformation of the jaw arch in the case of bilateral clefts is much more difficult, but it has a greater importance due to the difficulty of reconstruction of the muscular plan and severe deformations, what will persist if the segments can not be aligned. In the bilateral clefts, the lateral segments are displaced medially, and the medial segment is protruding. The purpose of preoperative orthodontic treatment is to reposition the lateral segments so that the medial segment can be coaxed between them together as a vault key of the maxillary arch. In order to study the occurrence of labia palatine cleft, we used eight groups of Wistar females rat, weighing between 200 and 250 grams, Each sample consists of 10 females rats. Most of the labial and palatine clefts are the result of multiple, genetic and non genetic factors, each producing a minor developmental defect, called multifactorial heritage;It can be represented by a model in which responsibility for a disease is a variable caused by a combination of genetic and environmental factors, The therapeutic outcome depends on the complexity of the malformation, on the moment of surgery and on the selection of the most modern techniques and equipment suitable for the patient.
机译:Labio-Maxilo-Palatine Clefts是由于宫内生命周期5-6周内遗传或非遗传因素的作用而发生的气候切割系统的胚胎发生障碍。裂缝是面部的先天性畸形组的一部分。它们从出生中出现,作为上唇的狭缝,硬腭和/或软腭。 Labio-Maxilo-Palatine塞拉特是目前的医学问题,特别是关于手术恢复;它们是先天性畸形,其特征在于上唇中没有物质和/或在腭穹窿中缺乏胚胎和/或腭芽在胚胎发育过程中缺乏沉着的唇缘突出的唇部,与唇缘缺乏完全唇裂,其也影响肺泡上颌拱。在这种畸形的情况下,比唇腭裂更严重,裂缝也影响骨骼结构(肺泡上颌拱,颊腭),使得口腔与鼻腔连通并防止在婴儿中吮吸婴幼儿。早期的手术恢复恢复了解剖结构的完整性,重新建立了令人不安的功能,根据年龄为孩子的言语教育和社会适应创造有利条件。在唇缘和前腭的主缝合之前应用该程序,以最小化上颌拱的分离的位错。在双边裂缝的情况下,颌骨畸形的矫正更加困难,但由于肌肉计划的重建和严重变形的难度,它具有更重要的意义,如果段不能对齐,将持续存在。在双侧馏分中,横向区段在内侧移位,内侧段突出。术前正畸治疗的目的是重新定位侧段,使得内侧段可以作为上颌拱的拱顶孔在一起。为了研究小腭裂的发生,我们使用了八组Wistar雌性大鼠,体重200至250克,每个样品由10只雌性大鼠组成。大多数唇缘和腭裂是多重,遗传和非遗传因素的结果,每种遗传和非遗传因素产生众所周知的遗传缺陷,称为多因素遗产;它可以由一种模型代表,其中疾病的责任是由组合引起的变量遗传与环境因素,治疗结果取决于畸形的复杂性,在手术的那一刻以及选择适合患者的最现代技术和设备的选择。

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