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l(f)r(sh)g2019-05-21 15:52
ժҪĿ̽ӑ1׼(x)𤸽ȱݲ(LAD-1)RCD18ױ_(d)ͻ׃Y(ji)RY,Ҏ(gu)ߌW(xu)Y,ʽ(x)g(sh)zy(c)׼(x)CD18,PCRy(c)丸ĸITGB2Y(ji)Ի,5q2,2(g)´r(sh)Ě,֮󷴏(f)жZگlװÓ3+q𷴏(f)ƤƤwȾ,t׼(x)(sh)@,(x),򵰰ߡܰͼ(x)(x)κ˼(x)CD18ӱ_(d)քe10.14%0.67%2.54%,жȱ,ĸ_(d)(քe96.01%99.05%96.58%;ĸքe91.12%92.98%81.43%)ITGB2@ʾ13̖(ho)@ӳF(xin)1(g)e(cu)xͻ׃c.1768TC(p.C590R),丸ĸͬλc(din)sͻ׃Y(ji)Փ(f)(yn)ƤwĤܛMȾ,Ěסt(f)lװÓ׼(x)(sh)@(x)򵰰ߵĻ辯LAD-1ʽ(x)g(sh)zy(c)׼(x)CD18ӿɿ\LAD-1,ITGB2\Ľ(bio)(zhn)
[Abstract]:Objective To study the clinical characteristics and the characteristics of CD18 protein expression in 1 (LAD-1) children with leukocyte adhesion molecule deficiency disease. Methods The clinical data, routine immunological screening and flow cytometry were used to detect the CD18 molecules on the surface of leukocytes, and the ITGB2 gene of the children and their parents were analyzed by PCR. Results The patients with male,2-month-old and 2-month-old were infected with umbilicus, followed by repeated pneumonia, otitis media, aphtha, gingivitis with deciduous teeth, and repeated rash, skin infection and wound healing after 3 + years of age. The total number of white blood cells in the children was significantly increased, and the number of neutrophils was the main and the immune globulin was increased. The expression of CD18 in lymphocytes, neutrophils and monocytes was 10.14%, 0.67% and 2.54%, respectively, and the parents were normal (96.01%, 99.05%, 96.58% and 91.12%, 92.98%, 81.43%, respectively). The ITGB2 gene analysis revealed 1 homozygous missense mutation in exon 13, c.1768 TC (p. C590R), both of which were heterozygous mutations at the same site. Conclusion Repeated severe skin and soft tissue infection, especially with umbilicus, delayed wound healing, and repeated gingivitis with deciduous teeth, the total number of white blood cells increased significantly, and the patients with increased immune globulin need to be alert to the LAD-1. The detection of CD18 on the surface of the white blood cell by flow cytometry can be used for the rapid diagnosis of LAD-1 and the analysis of the ITGB2 gene is the gold standard for diagnosis.
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𡿣ؑcпί(hu)˜I(y)cϿƼ(chung)Œ(xing)(cstc2015shmszx120028) 2014ҹИI(y)Ќ(xing)(201402012)
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