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La preeclampsia, el sistema inmune y la placenta 子痫前期、免疫系统和胎盘
Pub Date : 2023-09-10 DOI: 10.22201/fm.24484865e.2023.66.5.01
Teresa I. Fortoul van der Goes
The miracle of life is a topic that has been approached from different perspectives. Although budding human life is complex, perfect in its development program, it may go unnoticed by many. During medical practice there is an opportunity to care for and protect her. The recent knowledge about the early evolutionary stages of embryonic human life is astonishing. However, it is at this vulnerable stage of life that problems arise that can make the difference between life and death. Preeclampsia is a serious complication of pregnancy with deadly consequences for the mother and baby.
生命的奇迹是一个从不同角度探讨的话题。虽然萌芽中的人类生命在其发展计划中是复杂而完美的,但它可能被许多人忽视。在行医期间,有机会照顾和保护她。最近关于人类胚胎早期进化阶段的知识是惊人的。然而,正是在生命的这个脆弱阶段,出现的问题可能会导致生与死的不同。先兆子痫是一种严重的妊娠并发症,对母亲和婴儿都有致命的后果。
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引用次数: 0
Aspectos inmunológicos de preeclampsia 子痫前期的免疫学方面
Pub Date : 2023-09-10 DOI: 10.22201/fm.24484865e.2023.66.5.02
Arturo Cérbulo-Vázquez, Jose Anaya Herrera, Yolanda Flores-Cánovas, Carlos Gabriel Briones-Vega, Berenice Zavala-Barrios, Raúl Carrillo-Esper, Manuel Díaz de León Ponce, Jesús Carlos Briones-Garduño
Preeclampsia is a pathology with high morbidity and mortality worldwide. In this disease, the placenta is an organ of shock where inflammation and the immune response generate the damage that results in the characteristic clinical scenario. The classic triad in preeclampsia is made up of hypertension, edema, and proteinuria, so it is thought that the endothelium must be affected by inflammatory-immunological activity. The immune system acts in the development of pregnancy and does so at different times and regulating physiologically. Both, cellular and humoral components of the innate and acquired response have been studied in patients with preeclampsia and it has been determined that their participation is decisive in the pathophysiology of this disease. The involvement of the immune system in the pathophysiology of preeclampsia reaches a high level of complexity since it interacts with other systems (coagulation, renal, cardiovascular and endocrinological among others) thus favoring the disease. For this reason, treatment must be comprehensive, with a holistic vision of the condition and requires a multidisciplinary team that acts harmoniously to achieve the greatest therapeutic success with the least frequency of sequelae for the mother-fetus or mother-newborn dyads. During pregnancy, the so-called "immunological tolerance of pregnancy" develops, in this state of immunological tolerance the B and T cells can recognize specific antigens (for example, the paternal ones) and later activate and generate the immune response, which is why preeclampsia could being considered an autoimmune pathology, where the loss of immunological tolerance would be the cornerstone of pathophysiology, knowing how to limit or regulate this abnormal cell activation could help to propose new therapeutic approaches and thus control this disease.
子痫前期是世界范围内发病率和死亡率高的一种病理。在这种疾病中,胎盘是一个休克器官,炎症和免疫反应产生损伤,导致典型的临床情况。子痫前期典型的三联征是由高血压、水肿和蛋白尿组成的,因此认为内皮细胞一定受到炎症免疫活动的影响。免疫系统在怀孕的发展过程中起作用,并在不同的时间和生理上进行调节。先天和获得性反应的细胞和体液成分已经在子痫前期患者中进行了研究,并且已经确定它们的参与在该疾病的病理生理学中起决定性作用。由于免疫系统与其他系统(凝血系统、肾脏系统、心血管系统和内分泌系统等)相互作用,因此免疫系统参与子痫前期的病理生理学达到了高度的复杂性,从而有利于该疾病的发生。由于这个原因,治疗必须是全面的,对病情有一个整体的看法,需要一个多学科的团队协调行动,以达到最大的治疗成功,对母亲-胎儿或母亲-新生儿二联体的后遗症最少的频率。在怀孕期间,所谓的“妊娠免疫耐受”发展起来,在这种免疫耐受状态下,B细胞和T细胞可以识别特定的抗原(例如,父亲的抗原),然后激活并产生免疫反应,这就是为什么先兆子痫可以被认为是一种自身免疫病理,免疫耐受的丧失将是病理生理学的基石。了解如何限制或调节这种异常的细胞激活可以帮助提出新的治疗方法,从而控制这种疾病。
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引用次数: 0
Obstrucción intestinal secundario a vólvulo de sigmoides en un paciente joven. Reporte de un caso 一名年轻患者继发性乙状结肠旋流性肠梗阻。报告个案
Pub Date : 2023-09-10 DOI: 10.22201/fm.24484865e.2023.66.5.05
Andrés Manuel Aguilar Jaramillo, Ricardo Bautista de la Cruz, José Antonio Bautista Sánchez, Luis Cruz Benítez, Daniel Nazario Cruz, Dafne Thamara Ayala Dávila
Sigmoid volvulus occurs due to a torsion of the colonic mes¬enteric axis, it has a multifactorial and controversial etiology, and its pathophysiology is not yet clear. Presenting a clinical picture of non-specific onset and later signs and symptoms of intestinal occlusion, its diagnosis is established with computed tomography with a sensitivity and specificity greater than 90%. Management will depend on the clinical condition of the patient. Clinical case: A 29-year-old man with a history of Asperger syndrome. He referred 7 days prior to admission with dif¬fuse cramping pain, associated with abdominal distension and oral intolerance. He went to the hospital for evaluation where a computed tomography was performed with air-fluid levels, torsion of the inferior mesenteric artery with a whirl¬wind appearance. Exploratory laparotomy was performed, finding a dilated and volvulated sigmoid with perforation at the rectosigmoid junction. A sigmoidectomy with colorectal anastomosis was performed. On the fifth day, he presented data of inflammatory response with acute abdomen, enter¬ing exploratory laparotomy finding anastomosis dehiscence, Hartmann procedure was performed. The patient presented septic shock, died 24 hours after surgery. Discussion: The presentation of sigmoid volvulus generally occurs in people older than 70 years, few cases are described in young people and are related to intestinal dysmotility dis¬ease, the patient did not have predisposing factors, the diag¬nosis is established with characteristic images of the disease such as whirlwind image, surgical management is decided by performing resection with colorectal anastomosis. Conclusion: Intestinal occlusion due to sigmoid volvulus is an infrequent pathology in young people and with non-specific symptoms. When faced with a patient presenting evidence of intestinal occlusion, this should be appropriately addressed, especially in patients who have debuted with insidious and persistent symptoms of abdominal pain secondary to intestinal occlusion, whether they are young with or without risk factors.Keywords: Sigmoid volvulus; whirlwind sign; abdominal pain; intestinal obstruction.
乙状结肠扭转是由结肠肠轴扭转引起的,其病因多因素且有争议,其病理生理机制尚不清楚。其临床表现为肠道闭塞的非特异性发病和后来的体征和症状,其诊断通过计算机断层扫描建立,敏感性和特异性大于90%。治疗将取决于病人的临床情况。临床病例:29岁男性,有阿斯伯格综合症病史。患者入院前7天出现弥漫性绞痛,伴有腹胀和口腔耐受不良。他去医院做了评估,在那里进行了计算机断层扫描,显示了空气-液体水平,肠系膜下动脉扭曲,呈旋涡状。剖腹探查,发现乙状结肠扩张和扭转,并在直肠乙状结肠连接处穿孔。行乙状结肠切除术并结直肠吻合术。第5天出现急腹症炎症反应,开腹探查发现吻合口裂开,行Hartmann手术。患者出现感染性休克,术后24小时死亡。讨论:乙状结肠扭转多见于70岁以上老年人,青年少见,与肠道运动障碍疾病有关,患者无易感因素,根据疾病的特征性影像如旋风像确定诊断,手术处理以结肠吻合术切除决定。结论:乙状结肠扭转引起的肠阻塞在年轻人中是一种罕见的病理,无特异性症状。当面对有肠道闭塞证据的患者时,应该适当地解决这一问题,特别是对于首次出现隐性和持续性腹痛继发于肠道闭塞的患者,无论他们是年轻的,是否有危险因素。关键词:乙状结肠扭转;旋风标志;腹痛;肠梗阻。
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引用次数: 0
Oclusión Intestinal en paciente Renal Crónico secundario a Bezoar de Telas. Reporte de un Caso Clínico. 继发于牛粪网的慢性肾病患者肠闭塞。临床病例报告。
Pub Date : 2023-09-10 DOI: 10.22201/fm.24484865e.2023.66.5.03
Jesús Gerardo Valencia Martínez, Pricila Viridiana Ochoa Arias, Walther Espinoza Anguiano, Ricardo Reynoso González, Mariana Ángeles Santillán, Viridiana Aja Sixto
The “bezoar” are conglomerates of inedible materials ingest¬ed voluntarily or involuntarily, which are not digested and are unable to pass through the intestinal tract. They mainly affect young women or adolescents who present the phenomenon called “pica”, despite the fact that a high prevalence of this phenomenon of “pica” has been registered in patients with chronic kidney disease, it has been little studied. Clinical case: A 35-year-old male with CKD KDIGO-5 under¬going peritoneal dialysis treatment, which was found to have a transoperative “plastic bezoar” (laparotomy for intestinal occlusion) 10 cm from the ileocecal valve. The patient died due to complications of his pathology. Discussion: the clinical case raises the need to search for behaviors such as pica in patients with CKD, as well as to develop the suspicion to the surgeon, since patients generally hide or ignore reporting foreign material phagia. Keywords: Plastic Bezoar, Intestinal Occlusion, Chronic Kidney Disease, pica, dialysis
“牛黄”是由自愿或非自愿摄入的不可食用物质组成的聚集体,这些物质不会被消化,也无法通过肠道。它们主要影响出现异食癖(pica)现象的年轻女性或青少年,尽管事实上这种异食癖(pica)现象在慢性肾病患者中发病率很高,但对其研究甚少。临床病例:35岁男性CKD患者KDIGO-5,行腹膜透析治疗,经手术发现距回盲瓣10 cm处有“塑料牛黄”(开腹治疗肠闭塞)。病人死于病理并发症。讨论:该临床病例提示需要在CKD患者中寻找异食癖等行为,并向外科医生提出怀疑,因为患者通常隐藏或忽略报告异物吞噬。关键词:塑料牛黄,肠道闭塞,慢性肾病,异食癖,透析
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引用次数: 0
Destete fallido de la ventilación mecánica. Algunas consideraciones 机械通风断奶失败。一些注意事项
Pub Date : 2023-08-31 DOI: 10.15446/revfacmed.v70n4.110581
Agamenon Quintero-Villarreal
La tecnología ha puesto al alcance de los profesionales médicos equipos de ventilación mecánica y monitoreo más sofisticados para el mantenimiento de la función respiratoria. Por lo tanto, cada día existen más opciones para tratar a los pacientes que ingresan a las unidades de cuidado intensivo (UCI) y requieren asistencia mecánica ventilatoria invasiva, sobre todo aquellos con sepsis grave y choque séptico.
这项技术为医疗专业人员提供了更复杂的机械通气和监测设备,以维持呼吸功能。因此,对于进入重症监护病房(icu)并需要有创性机械通气辅助的患者,特别是严重脓毒症和脓毒症休克患者,治疗的选择越来越多。
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引用次数: 0
Effect of physical exercise on heart rate variability in adults with overweight or obesity: A systematic review and meta-analysis 体育锻炼对超重或肥胖成人心率变异性的影响:系统回顾和荟萃分析
Pub Date : 2023-08-24 DOI: 10.15446/revfacmed.v71n4.107632
Lubin Betancur-Sepulveda, Jhon Freddy Ramírez-Villada, Carlos Mario Arango-Paternina
Introduction: Cardiac autonomic dysfunction is a cardiovascular risk factor associated with various health conditions, mainly in overweight and obese individuals. In this regard, heart rate variability (HRV) is one of the tools that allow the evaluation of the activity of the autonomic nervous system (ANS), facilitating the physiological characterization and diagnosis of any individual. Objective: To determine the effect of physical exercise on heart rate variability (HRV) in adults (>18 years old) with overweight or obesity. Materials and methods: Systematic review. Cochrane, Medline, Embase, Lilacs, and PEDro databases were systematically searched using the following search strategy: types of study: randomized controlled trials (RCTs) assessing the effect of exercise-based interventions on HRV parameters in adults with overweight or obesity; publication period: January 2015 to June 2021; Language: English; search terms: MeSH terms combined with Boolean operators “AND” and “OR”. The review protocol was registered in PROSPERO (code: CRD42021224027). The risk of bias was assessed using the Cochrane risk of bias assessment tool. A random-effects meta-analysis was performed to estimate the pooled effect for each outcome variable (HRV parameter) when the pooling of data was possible. Subgroup analyses were also performed to make comparisons between the different interventions. A significance level of p<0.05 was considered. Results: The initial searches yielded 2650 studies; of these,only 10 RCTs met the inclusion criteria. There were no statistically significant differences between the intervention and control groups in terms of changes in the HRV parameters: standard deviation of normal-to-normal R-R (NNN) intervals (SDNN): weighted mean difference (WMD)=1.30, 95%CI:-5.93-8.53, p-value=0.72); root mean square of successive RR intervals differences (RMSSD): (WMD=0.79, 95%CI:-0.29-1.87, p-value=0.15); high frequency (HF): (WMD=6.67, 95%CI:1.71-11.63, p-value=0.008), and low frequency (LF): (WMD=-0.32, 95%CI:-0.73-0.10, p-value=0.13). Conclusions: Physical exercise did not affect any of the HRV parameters studied in adults with overweight or obesity.
心脏自主神经功能障碍是一种与多种健康状况相关的心血管危险因素,主要发生在超重和肥胖人群中。在这方面,心率变异性(HRV)是允许评估自主神经系统(ANS)活动的工具之一,有助于任何个体的生理特征和诊断。目的:探讨体育锻炼对18岁超重或肥胖成人心率变异性(HRV)的影响。材料与方法:系统综述。采用以下搜索策略对Cochrane、Medline、Embase、Lilacs和PEDro数据库进行系统搜索:研究类型:随机对照试验(RCTs),评估基于运动的干预对超重或肥胖成人HRV参数的影响;出版期限:2015年1月至2021年6月;语言:英语;搜索词:网格词与布尔运算符“与”和“或”的组合。审查方案已在PROSPERO中注册(代码:CRD42021224027)。使用Cochrane偏倚风险评估工具评估偏倚风险。进行随机效应荟萃分析,以在可能合并数据时估计每个结局变量(HRV参数)的合并效应。还进行了亚组分析以比较不同干预措施之间的差异。考虑p < 0.05的显著性水平。结果:最初的搜索产生了2650项研究;其中,只有10项rct符合纳入标准。干预组与对照组HRV参数变化差异无统计学意义:正态至正态R-R (NNN)区间标准差(SDNN):加权平均差(WMD)=1.30, 95%CI:-5.93 ~ 8.53, p值=0.72;连续RR区间差的均方根(RMSSD):(WMD=0.79, 95%CI:-0.29-1.87, p值=0.15);高频(HF): WMD=6.67, 95%CI:1.71 ~ 11.63, p值=0.008),低频(LF): WMD=-0.32, 95%CI:-0.73 ~ 0.10, p值=0.13)。结论:体育锻炼对超重或肥胖成人的HRV参数没有影响。
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引用次数: 0
Preferencia sobre métodos tradicionales y/o modernos en la enseñanza de anatomía 对传统和/或现代解剖学教学方法的偏好
Pub Date : 2023-07-28 DOI: 10.37345/23045329.v1i34.83
Diego Alejandro Morales Marroquín, Favio Adrián Reyna Carrera
La anatomía es una de las ciencias más críticas en medicina, ya que posee una importancia clave en la formación clínica de un médico. A través del tiempo los métodos de aprendizaje han variado y gracias a los avances tecnológicos, la anatomía guiada por realidad virtual ha emergido como un método de aprendizaje novedoso e interactivo con los estudiantes de medicina. El objetivo del presente estudio fue identificar el método de aprendizaje de anatomía preferido por estudiantes de tercer año de la Facultad de Medicina de la Universidad Francisco Marroquín, para lo cual se realizó un estudio descriptivo transversal, en 36 estudiantes en el período de septiembre del 2022. Los resultados demostraron que la inmersión con el uso de anatomía guiada por realidad virtual aumenta el interés por el curso, facilita y mejora la comprensión del contenido educativo y produce una mayor participación en clase. En conclusión, los estudiantes mostraron una mayor preferencia por el método de aprendizaje de anatomía guiada por realidad virtual en contraste con los métodos tradicionales de enseñanza (libros, imágenes 2D, etc.).
解剖学是医学中最重要的科学之一,在医生的临床培训中起着至关重要的作用。随着时间的推移,学习方法发生了变化,由于技术的进步,虚拟现实引导解剖已经成为一种新的互动学习方法与医学生。本研究的目的是确定弗朗西斯科大学医学院marroquin三年级学生喜欢的解剖学学习方法,为此我们在2022年9月期间对36名学生进行了横断面描述性研究。结果表明,虚拟现实引导解剖的沉浸式使用增加了课程的兴趣,促进和提高了对教育内容的理解,并产生了更大的课堂参与度。综上所述,与传统的教学方法(书籍、2D图像等)相比,学生更喜欢虚拟现实引导的解剖学学习方法。
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引用次数: 0
Descripción Clínica de los Pacientes Pediátricos Oncológicos con Neutropenia Febril Ingresados a la Unidad de Cuidados Intensivos de la Unidad Nacional de Oncología Pediátrica 本研究的目的是评估在美国儿科肿瘤科住院的发热性中性粒细胞减少症儿童肿瘤患者的临床特征。
Pub Date : 2023-07-28 DOI: 10.37345/23045329.v1i34.84
Gabriela Marina Gavidia Mayora, Amanda Lucía Armendáriz Ortíz, Ricardo Alfredo Mack Rivas
Objetivo: Describir las características clínicas de los pacientes pediátricos oncológicos que fueron diagnosticados con Neutropenia Febril (NF) ingresados por primera vez a la Unidad de Cuidados Intensivos (UCI) de la Unidad Nacional de Oncología Pediátrica (UNOP). Métodos:  Estudio descriptivo y retrospectivo, se caracteriza un total de 211 pacientes que desarrollaron NF y requirieron ingreso a la UCI, entre los años 2017 a 2021. Resultados: La edad promedio fue de 8 años, 46% fueron hombres y 54% mujeres. Se presentó neutropenia severa en el 72.77% de los casos y la leucemia (81.99%) fue el diagnóstico oncológico destacado. Dentro de todos los tratamientos, el 38.39% de los pacientes se encontraban en fase de inducción. En un 33.18% se logró identificar un agente infeccioso asociado. Las bacterias de tipo Gram-negativo fueron el agente infeccioso causal más frecuente (13.74%). La media del tiempo de estancia en UCI fue de 6.75 ± 5.79 días. Un 91.62% de pacientes no ameritaron ventilación mecánica y la complicación más frecuentemente asociada a NF fue Sepsis en un 65.88% de los casos. Conclusión: La mayoría de los casos de Neutropenia Febril son severos, las neoplasias hematológicas (LLA y LMA) son la enfermedad de base más frecuente para el desarrollo de NF y las bacterias de tipo Gram-negativo son el agente infeccioso más frecuente. La mayoría de los pacientes no ameritan ventilación mecánica y las complicaciones más frecuentemente asociadas son Sepsis y Neumonía.
本研究的目的是描述在国家儿科肿瘤单位(UNOP)的重症监护病房(icu)首次被诊断为发热性中性粒细胞减少症(NF)的儿科肿瘤患者的临床特征。方法:描述性和回顾性研究,对2017年至2021年共211例发生NF并需要icu的患者进行特征分析。结果:8岁的平均年龄,有46%和54%的男女。在一项研究中,72.77%的患者表现为严重中性粒细胞减少,白血病(81.99%)是主要的肿瘤诊断。在所有治疗中,38.39%的患者处于诱导阶段。33.18%的人成功地确定了相关的感染源。革兰氏阴性菌是最常见的致病病原体(13.74%)。患者在icu的平均停留时间为6.75±5.79天。91.62%的患者不需要机械通气,65.88%的病例中与NF相关的最常见并发症是败血症。结论:发热性中性粒细胞减少症的病例多为严重,血液学肿瘤(all和aml)是NF发展最常见的基础疾病,革兰氏阴性细菌是最常见的感染源。大多数患者不需要机械通气,最常见的相关并发症是败血症和肺炎。
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引用次数: 0
Obesidad : Un breve repaso a su tratamiento 肥胖:对其治疗的简要回顾
Pub Date : 2023-07-28 DOI: 10.37345/23045329.v1i34.96
Jorge Tulio Rodríguez
Controlar el peso excesivo ha sido reconocido como una mejora en la calidad de vida. La obesidad es considerada como una enfermedad en la que hay una respuesta inadecuada del cerebro para evitar la emaciación.  El consumo de calorías en excesodemasía produce acumulación excesiva de grasa corporal. El sobrepeso (no obesidad), se define como IMC de 25.0 a 29.9. Obesidad clase 1 (de bajo riesgo), si el IMC es de 30 a 34.9. Obesidad clase 2 (riesgo moderado), si el IMC es de 35 a 39.9. Obesidad clase 3 (de alto riesgo), si el IMC es igual o mayor a 40.
控制超重被认为是生活质量的提高。肥胖被认为是一种大脑对防止肥胖反应不足的疾病。过多的卡路里消耗会导致身体脂肪的过度积累。超重(不是肥胖)的定义是bmi在25.0到29.9之间。1级肥胖(低风险),如果bmi在30到34.9之间。2级肥胖(中度风险),bmi为35 - 39.9。3级肥胖(高危),如果bmi等于或大于40。
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引用次数: 0
Fibrodisplasia Osificante Progresiva: Reporte de Primer Caso Guatemalteco 进行性骨化纤维发育不良:危地马拉第一例病例报告
Pub Date : 2023-07-28 DOI: 10.37345/23045329.v1i34.92
Marcela Elizabeth Orozco Orozco, Anna Yurrita Pocasangre, María Antonieta Sandoval Vargas, Julio Rafael Cabrera Valverde
La Fibrodisplasia Osificante Progresiva (FOP) es una enfermedad rara, compleja, de herencia autosómica dominante, causada por una mutación heterocigota del gen ACVR1 en el cromosoma 2q24 (OMIM 135100), con una prevalencia de 1 en 2 millones en todo el mundo. Se caracteriza por osificaciones heterotópicas progresivas que involucran músculo esquelético, fascias, tendones y ligamentos. El diagnóstico se basa en la historia clínica y lesiones en los tejidos blandos. Los estudios de imágenes respaldan la identificación de dichas osificaciones. Se confirma mediante el análisis de ADN del gen ACVR1 por medio de secuenciación. Actualmente no existe una terapia definitiva y curativa. El objetivo de este artículo es presentar el caso clínico de una niña de 3 años con el diagnóstico clínico y radiológico de FOP.
进行性骨化纤维发育不良(FOP)是一种罕见的、复杂的常染色体显性遗传疾病,由2q24染色体(OMIM 135100)上的ACVR1基因杂合突变引起,全球发病率为1 / 200万。其特征是进行性异位骨化,累及骨骼肌、筋膜、肌腱和韧带。诊断依据是病史和软组织病变。影像学研究支持这些骨化的识别。通过测序分析ACVR1基因的dna来确认。目前还没有明确的治疗方法。本研究的目的是评估一名患有FOP的3岁女孩的临床和放射学诊断。
{"title":"Fibrodisplasia Osificante Progresiva: Reporte de Primer Caso Guatemalteco","authors":"Marcela Elizabeth Orozco Orozco, Anna Yurrita Pocasangre, María Antonieta Sandoval Vargas, Julio Rafael Cabrera Valverde","doi":"10.37345/23045329.v1i34.92","DOIUrl":"https://doi.org/10.37345/23045329.v1i34.92","url":null,"abstract":"La Fibrodisplasia Osificante Progresiva (FOP) es una enfermedad rara, compleja, de herencia autosómica dominante, causada por una mutación heterocigota del gen ACVR1 en el cromosoma 2q24 (OMIM 135100), con una prevalencia de 1 en 2 millones en todo el mundo. Se caracteriza por osificaciones heterotópicas progresivas que involucran músculo esquelético, fascias, tendones y ligamentos. El diagnóstico se basa en la historia clínica y lesiones en los tejidos blandos. Los estudios de imágenes respaldan la identificación de dichas osificaciones. Se confirma mediante el análisis de ADN del gen ACVR1 por medio de secuenciación. Actualmente no existe una terapia definitiva y curativa. El objetivo de este artículo es presentar el caso clínico de una niña de 3 años con el diagnóstico clínico y radiológico de FOP.","PeriodicalId":21295,"journal":{"name":"Revista de la Facultad de Medicina","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-07-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73065368","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Revista de la Facultad de Medicina
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