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Complete Cleft Palate: A New Scheme Of Treatment

机译:完全性Pal裂:新的治疗方案

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The problems of complete cleft palate still represent a great challenge because of the potential associated sequalae and complications with the current treatment scheme which necessitated finding out a new scheme of treatment that can minimize these problems. Introduction Complete cleft palate is a real exhaust for the patient, his family and the treating team. The treatment does not end by closing the cleft, but may extend up to the age of 18 years or more. The increased incidence of complications as speech problems, middle ear infections and palatal fistula let us investigate this problem and compare between two techniques of closure as well as deciding the time of surgery.IncidenceCleft lip and cleft palate are the most common congenital anomalies of the head and neck occurring as 1 in 750 live births. In Orientals it is 1:500, in Caucasians it is 1:1000 and in black Americans it is 0.4:1000. The recent views suggest that clefts are due to multifactorial etiology involving many genes and environmental factors. The isolated cleft palate is more heterogeneous. Associated anomalies are seen in cases as Robin syndrome and Fallot's tetralogy. Drugs during pregnancy, consanguinity, and exposure to radiation are common environmental causes in the etiology (Decker and Du Plessis, 1980: His 1901: El-Rakhawy,1978: Stark and Kernahan 1959: Stark, 1954: Wyszynski et al 1997)
机译:完全裂pa问题仍然是一个巨大的挑战,因为当前治疗方案可能伴有角叉骨和并发症,因此有必要寻找一种新的治疗方案以最大程度地减少这些问题。简介完全裂c对于患者,他的家人和治疗团队来说是真正的排气。治疗不会以闭合裂口而告终,但可延长至18岁或以上。言语问题,中耳感染和pa瘘等并发症的发生率不断上升,这使我们可以调查这个问题,并比较两种闭合术和决定手术时间的情况。发病率唇left裂和c裂是头部最常见的先天性异常750例活产中有1例发生在颈部和颈部。在东方人中是1:500,在白种人中是1:1000,在美国黑人中是0.4:1000。最近的观点表明,left裂是由于涉及许多基因和环境因素的多因素病因引起的。孤立的c裂更不均匀。在病例中,伴有异常现象的是罗宾综合症和法洛氏四联症。在病因学中,怀孕,血缘和暴露于辐射期间的药物是常见的环境原因(Decker和Du Plessis,1980年:他的1901年:El-Rakhawy,1978年:Stark和Kernahan 1959年:Stark,1954年:Wyszynski等1997)

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