Academic Journal
甲基丙二酸尿症合并先天性肾上腺皮质增生症1例报告 ; Methylmalonic aciduria combined with congenital adrenal hyperplasia:a case report
| العنوان: | 甲基丙二酸尿症合并先天性肾上腺皮质增生症1例报告 ; Methylmalonic aciduria combined with congenital adrenal hyperplasia:a case report |
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| المؤلفون: | 刘玉鹏, 丁圆, 李溪远, 宋金青, 王峤, 张尧, 刘戈力, 王立文, 杨艳玲 |
| المساهمون: | 北京大学第一医院儿科 北京 100034, 天津医科大学总医院儿科 天津 300052, 首都儿科研究所附属儿童医院神经科 北京 100020 |
| المصدر: | 知网 ; 万方 ; CSCD ; http://d.g.wanfangdata.com.cn/Periodical_lcekzz201603013.aspx |
| بيانات النشر: | 临床儿科杂志 |
| سنة النشر: | 2016 |
| المجموعة: | Peking University Institutional Repository (PKU IR) / 北京大学机构知识库 |
| مصطلحات موضوعية: | 甲基丙二酸尿症, MUT基因, 先天性肾上腺皮质增生症, 21羟化酶缺乏症, CYP21A2基因, methylmalonic aciduria, MUT gene, congenital adrenal hyperplasia, 21-hydroxylase deficiency, CYP21A2 gene |
| الوصف: | 目的：探讨罕见的甲基丙二酸尿症合并先天性肾上腺皮质增生症患儿的诊疗方法。方法分析1例甲基丙二酸尿症变位酶缺乏合并21羟化酶缺乏症患儿的临床及实验室资料。结果患儿，男，生后3个月起病，接种疫苗及高蛋白饮食后出现喂养困难、腹泻、代谢紊乱及智力运动发育倒退，1岁8个月时确诊为甲基丙二酸尿症，治疗后好转。5岁后出现性早熟表现，确诊为21羟化酶缺乏症男性化型。基因证实MUT基因存在c.866G?>?C和c.2179C?>?T两个突变，CYP21A2基因存在c.188A?>?T和c.518T?>?A两个已知突变。结论遗传代谢病及内分泌病临床表现复杂，鲜有病例共患多种疾病，该患儿共患甲基丙二酸尿症及21羟化酶缺乏症两种罕见疾病。 ; Objective To explore the diagnosis and treatment of a rare case of methylmalonic aciduria combined with congenital adrenal hyperplasia. Methods The clinical and laboratory data of the first case of methylmalonyl CoA mutase deifcient methylmalonic aciduria combined with 21-hydroxylase deifciency in China were analyzed. Results The male patient with age of onset at 3 months presented with feeding dififculty, diarrhea, metabolic acidosis, and psychomotor retardation after polio vaccination or high protein diet. At one year and 8 months of age, methylmalonic aciduria was diagnosed, and the patient was clinically improved after treatment. At 5 years of age, precocious puberty was noticed, and virilizing form of 21-Hydroxylase deifciency was diagnosed. Genetic testing conifrmed 2 known mutations in MUT gene (c.866G?>?C, c.2179C?>?T) and 2 known mutations in CYP21A2 gene (c.188A?>?T, c.518T?>?A). Conclusions The clinical manifestations of inherited metabolic disorders and endocrine diseases are complex and it is rare that multiple disorders occurred simultaneously in one patient. This male patient has two rare diseases, methylmalonic aciduria and 21-hydroxylase deifciency. ; “十二五”国家科技支撑计划项目(No.2012BAI03B02，2012BAI09B04)；儿科遗传性疾病分子诊断与研究北京市重点实验室 ; 中文核心期刊要目总览(PKU) ; 中国科技核心期刊(ISTIC) ; 中国科学引文数据库(CSCD) ; 3 ; 208-211 ; 34 |
| نوع الوثيقة: | journal/newspaper |
| اللغة: | Chinese |
| تدمد: | 1000-3606 |
| Relation: | 临床儿科杂志.2016,34,(3),208-211.; 1404578; http://hdl.handle.net/20.500.11897/441427 |
| DOI: | 10.3969/j.issn.1000-3606.2016.03.013 |
| الاتاحة: | https://hdl.handle.net/20.500.11897/441427 https://doi.org/10.3969/j.issn.1000-3606.2016.03.013 |
| رقم الانضمام: | edsbas.A16DEB3 |
| قاعدة البيانات: | BASE |
| تدمد: | 10003606 |
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| DOI: | 10.3969/j.issn.1000-3606.2016.03.013 |