2型Crigler-Najjar综合征的产妇结局:病例报告

IF 0.9 4区 计算机科学 Q3 COMPUTER SCIENCE, THEORY & METHODS International Journal of Parallel Programming Pub Date : 2021-04-15 DOI:10.18231/J.IJPP.2021.015
Amol Deore, Vijay Ahirrao
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引用次数: 0

摘要

Crigler-Najjar综合征2型[CN-2]是一种罕见的遗传性疾病,其特征是非溶血性非结合性高胆红素血症。它是由UGT1A1基因的五个外显子中的一个突变引起的,该基因编码肝尿苷二磷酸葡糖基转移酶-1,该酶是结合胆红素并通过胆汁进一步从体内排出胆红素所必需的。除了黄疸外,受影响的人通常没有症状,调查显示有孤立的间接高胆红素血症。可以通过评估对苯巴比妥的反应来降低胆红素水平,从而方便地进行诊断。基因检测证实了Crigler-Najjar综合征的发现。UGT1A1至少有20种不同的突变与CN-2有关;全部编码胆红素尿苷二磷酸葡糖醛酸基转移酶-1,其酶活性显著降低但可检测。CN-2中的胆红素浓度通常较低,苯巴比妥可将血浆胆红素水平降至3-5 mg/dL。尽管在CN-2中不常见,但胆红素脑病在所有年龄段都有发生,通常与暂时性降低血浆胆红素浓度高于基线的因素有关,如压力、长期禁食、流感等并发疾病。因此,通常建议使用苯巴比妥治疗。CN-2是罕见的,只有少数妊娠与这种情况的报道。本病例研究的目的是报告一例罕见的妊娠期母体CN-2病例,并评估该疾病患者的妊娠是否安全。一位患有CN-2的29岁母亲通过自然阴道分娩产下了一名女婴,没有出现并发症。新生儿有轻度未结合高胆红素血症,通过光疗和清晨阳光进行进一步治疗。可以得出结论,CN-2不需要禁止妊娠。关键词:高胆红素血症,光疗,UGT1A1基因,黄疸,葡萄糖醛酸化。
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Maternal outcome of Crigler-Najjar syndrome type-2: Case report
Crigler-Najjar Syndrome type 2 [CN-2] is an uncommon inherited disorder characterized by non-hemolytic unconjugated hyperbilirubinemia. It is caused by mutations in one of the five exons of the UGT1A1 gene which codes for the enzyme hepatic uridine diphosphate glucoronosyl transferase-1, required for the conjugation and further excretion of bilirubin from the body via bile. Affected people are usually asymptomatic apart from jaundice and investigations reveal isolated indirect hyperbilirubinemia. It can be conveniently diagnosed by evaluating the response to phenobarbital in terms of reduction in bilirubin levels. Genetic testing confirms the finding of Crigler-Najjar syndrome. At least 20 different mutations of UGT1A1 have been associated with CN-2; all encode a bilirubin-uridine diphosphate glucuronosyl transferase-1 with markedly reduced but detectable enzymatic activity. Bilirubin concentrations are typically lower in CN-2, and plasma bilirubin levels can be reduced to 3 to 5 mg/dL by phenobarbital. Although uncommon in CN-2, bilirubin encephalopathy has occurred at all ages, typically associated with factors that temporarily elevation the plasma bilirubin concentration above baseline e.g. stress, prolonged fasting, an intercurrent illness like influenza. For this reason, phenobarbital therapy is often recommended. CN-2 is infrequent, and only a few pregnancies with this condition have been reported. The objective of the case study is to report a rare case of maternal CN-2 in the pregnancy and to evaluate whether pregnancy is safe in patients with the disease. A 29 years old mother with CN-2 had given birth to a baby girl by spontaneous vaginal delivery without complications. The newborn had mild unconjugated hyperbilirubinemia which was further treated by phototherapy and early morning sunlight. It can be concluded that that pregnancy need not be contraindicated in CN-2. Keywords: Hyperbilirubinemia, Phototherapy, UGT1A1 gene, Jaundice, Glucuronidation.
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来源期刊
International Journal of Parallel Programming
International Journal of Parallel Programming 工程技术-计算机:理论方法
CiteScore
4.40
自引率
0.00%
发文量
15
审稿时长
>12 weeks
期刊介绍: International Journal of Parallel Programming is a forum for the publication of peer-reviewed, high-quality original papers in the computer and information sciences, focusing specifically on programming aspects of parallel computing systems. Such systems are characterized by the coexistence over time of multiple coordinated activities. The journal publishes both original research and survey papers. Fields of interest include: linguistic foundations, conceptual frameworks, high-level languages, evaluation methods, implementation techniques, programming support systems, pragmatic considerations, architectural characteristics, software engineering aspects, advances in parallel algorithms, performance studies, and application studies.
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