Vater or vacterl can be referred term paper
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All surgeries were powerful and the diagnosis based on followup testing was good. (Yamashiro et approach., 2007)
Tracheoplasty was also carried out to get fourteen patients, seven of whom confirmed other indications of VATER relationship and the rest presented tracheal problems with out other VATER symptoms. (Fiore, Brown, Weber, Turrentine, 2005)the same treatment modality was used for all patients with the loss of only two patients. Follow up indicated this was a sound modality for treatment of tracheal defects in VATER organizations. Similarly, urinary tract renovation was deemed successful very safe for end-stage renal disease in babies. The overall sufferer survival charge was 95%. (DeFoor ou al., 2003) and, in another study, it had been shown that neurosurgical treatment was good 60% of times for hydrocephalus from VATER, which requests the experts to indicate that the prognosis of certain loss of life is not really true and that the patients who survived possess good diagnosis.
It would seem in that case that treatment modalities for VATER are no different from various other symptoms. That is because the symptoms are cared for. It will be most likely a while before the root cause of VATER – the genes (one or more) will be identified.
Al Kaissi, a., Bill Chehida, N., Safi, H., Nassib, In., Ben Ghachem, M., Gharbi, H., et al. (2006). Progressive congenital torticollis in VATER relationship syndrome. Backbone, 31(12), E376-378.
DeFoor, W., Minevich, At the., McEnery, P., Tackett, T., Reeves, G., Sheldon, C. (2003). Reduce urinary system reconstruction is secure and powerful in kids with end stage suprarrenal disease. Record of Urology, 170(2), 1497-1500.
Fiore, a. C., Brown, J. Watts., Weber, Capital t. R., Turrentine, M. W. (2005). Medical procedures of pulmonary artery tricing and tracheal stenosis. Ann Thorac Surg, 79(1), 38-46; discussion 38-46.
Fujishiro, E., Suzuki, Con., Sato, Capital t., Kondo, T., Miyachi, M., Suzumori, T. (2004). Characteristic findings intended for diagnosis of baby complicated with the VACTERL association and duodenal atresia Fetal Diagnostic Therapy, 19(2), 134-137.
Guerrier, D., Mouchel, T., Pasquier, L., Pellerin, I. (2006). The Mayer-Rokitansky-Kuster-Hauser syndrome (congenital absence of womb and vagina) – phenotypic manifestations and genetic techniques. J Negat Results Biomed, 5, 1 .
Kennelly, M. M., Moran, P. (2007). A clinical algorithm of prenatal associated with Radial Ray Defects with two and three dimensional ultrasound. Prenat Diagn, 27(8), 730-737.
Maschke, H. D., Seitz, W., Lawton, J. (2007). Radial longitudinal deficiency. M Am Acad Orthop Surg, 15(1), 41-52.
Mishra, a. (2007). Renal agenesis: record of an interesting case. Br J. Radiol, 80(956), e167-169.
Sunagawa, H., Kikuchi, a., Yoshida, T., Miya*****a, T., Takagi, K., Kawame, L., et ing. (2007). Dichorionic twin fetuses with VACTERL association. M Obstet Gynaecol Res, 33(4), 570-573.
Tercanli, S., Troeger, C., Fahnenstich, H., Hosli, I., Holzgreve, W. (2001). [Prenatal diagnosis and management in VACTERL association]. Z Geburtshilfe Neonatol, 205(2), 65-70.
Weisz, B., Achiron, R., Schindler, a., Eisenberg, V. L., Lipitz, T., Zalel, Y. (2004). Prenatal sonographic associated with hemivertebra. M Ultrasound Med, 23(6), 853-857.
Yamashiro, Meters., Nakamura, Y., Nomura, T.
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