Paragonimiasis pulmonar crónica en niño indígena kichwa contagiado en la amazonia ecuatoriana [0.03%]
厄瓜多尔亚马逊地区感染的基楚娃印第安儿童肺并殖吸虫病慢性期病例
Manuel Calvopina,Elías David Guaman-Charco,Jeremmy Erazo-Coello et al.
Manuel Calvopina et al.
La paragonimiasis es una parasitosis causada por el trematodo Paragonimus spp. La Organización Mundial de la Salud la considera una enfermedad tropical desatendida, clasificada como alimentaria, causada por la ingestión de crustáceos de ...
Metahemoglobinemia secundaria al uso de primaquina en un caso pediátrico de malaria [0.03%]
一例儿童疟疾病例使用伯氨喹导致的高铁血红蛋白血症
Sara Puerta,Hardenson Rodríguez
Sara Puerta
La metahemoglobinemia es el resultado del aumento de la concentración de metahemoglobina en la sangre, lo cual impide una adecuada liberación del oxígeno en los tejidos. Se considera una condición poco frecuente que requiere de una gran...
Julián Alfredo Fernández-Niño
Julián Alfredo Fernández-Niño
Nutritional status in pediatric patients with predominant antibody deficiency [0.03%]
以抗体缺乏为主的儿科患者的营养状况
Lina M Castaño-Jaramillo,Olga Rodríguez,Natalia Vélez-Tirado
Lina M Castaño-Jaramillo
Introduction: Predominant antibody deficiency is the most frequent group of innate immunity errors, but information about patients’ nutritional status is scarce. ...
Intra-mesenteric steroids for steroid-refractory graft-versus-host disease in pediatric patients: A safe option [0.03%]
腹膜内糖皮质激素用于儿科患者难治性移植物抗宿主病的安全有效性的研究
Ana M Aristizábal,Lina P Montaña,Jaiber Gutiérrez et al.
Ana M Aristizábal et al.
Introduction: Graft-versus-host disease is a serious complication after hematopoietic stem cell transplantation and is a major cause of death post-transplantation. Approximately 50% of acute graft-versus-host disease pati...
Severe immunodeficiency spectrum associated with NHEJ1 gene mutation: Cernunnos/XLF deficiency [0.03%]
非淋巴细胞末端连接缺陷蛋白基因突变所致严重免疫缺陷病：Cernunnos/XLF缺陷症
Ana María Navarro,Gabriela Mantilla,Jorge Andrés Fernández et al.
Ana María Navarro et al.
Cernunnos/XLF deficiency is a rare, severe combined immunodeficiency, inherited in an autosomal recessive pattern (OMIM number: 611290), related to the NHEJ1 gene. This gene participates in the DNA non-homologous end-joining pathway, repair...
Recommendations on vaccination in children and adolescents with inborn errors of immunity according to the expanded Colombian immunization program [0.03%]
哥伦比亚扩展免疫规划下自身免疫缺陷儿童与青少年疫苗接种推荐意见
Nathalia Cortés-Marín,Luis Miguel Sosa-Ávila,Andrés Felipe Arias et al.
Nathalia Cortés-Marín et al.
In this manuscript, we carried out an exhaustive analysis of the global recommendations for immunization in inborn errors of immunity patients. We examined the mechanisms of action and types of vaccines, and we described the vaccines includ...
Lymphoproliferation and hyper-IgM as the first manifestation of activated phosphoinositide 3-kinase δ syndrome: A case report [0.03%]
活化型磷脂酰肌醇-3,4,5-三磷酸激酶δ综合征的首发表现为淋巴细胞增殖和高IgM血症：1例报告
Mónica Fernandes-Pineda,Andrés F Zea-Vera
Mónica Fernandes-Pineda
Activated phosphoinositide 3-kinase δ syndrome is an inborn error of immunity due to mutations within the genes responsible for encoding PI3Kδ subunits. This syndrome results in an excessive activation of the phosphoinositide 3-kinase sig...
Standardization of the use of opsonized zymosan as stimulus in the 1,2,3-dihydrorhodamine technique for the assessment of neutrophil respiratory burst [0.03%]
用于评估中性粒细胞呼吸爆发的1,2,3-二氢罗丹明技术中以调理子念珠菌多糖作为刺激物的标准条件
Uriel Pérez-Blanco,Jenniffer Yissel Girón,Guillermo Juárez-Vega et al.
Uriel Pérez-Blanco et al.
Introduction: Chronic granulomatous disease is a defect in phagocytosis due to deficiency of gp91phox, p22phox, p47phox, p40phox, and p67phox (classic form of the disease). Recently, EROS and p40phox deficiency were descr...
Infections, autoimmunity and immunodeficiencies are the leading etiologies of non-cystic fibrosis bronchiectasis in adults from the southwest of Colombia [0.03%]
哥伦比亚西南部成人非囊性纤维化支气管扩张的主要病因是感染，自身免疫和免疫缺陷
Andrés F Zea-Vera,Carlos Andrés Rodríguez,Sebastián Giraldo et al.
Andrés F Zea-Vera et al.
Introduction: Non-cystic fibrosis bronchiectasis is a complex medical condition with multiple etiologies, characterized by chronic productive cough and radiologic evidence of airway lumen dilation and wall thickening. Ass...