青春期家族性甲状旁腺功能亢进伴CDC73基因种系移码突变1例

IF 1 Q4 ENDOCRINOLOGY & METABOLISM Clinical Pediatric Endocrinology Pub Date : 2015-10-01 DOI:10.1297/cpe.24.185
Takako Takeuchi, Y. Yoto, T. Tsugawa, H. Kamasaki, A. Kondo, J. Ogino, T. Hasegawa, N. Yama, Sawa Anan, S. Uchino, A. Ishikawa, A. Sakurai, H. Tsutsumi
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引用次数: 4

摘要

摘要一个13岁的男孩抱怨持续恶心,呕吐和体重减轻,高钙血症和完整甲状旁腺激素水平升高。计算机断层扫描证实甲状腺有两个肿瘤。经手术切除,病理证实为甲状旁腺瘤。由于他的姑姑和祖母都有甲状旁腺肿瘤病史,因此对他进行了遗传调查,并鉴定出CDC73基因的种系移码突变。对于有家族性甲状旁腺功能亢进风险的个体,包括无症状的个体,应进行CDC73基因分析,并应随访潜在的原发性甲状旁腺功能亢进和相关疾病,包括由此产生的甲状旁腺癌。
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An adolescent case of familial hyperparathyroidism with a germline frameshift mutation of the CDC73 gene
Abstract. A 13-yr-old boy who complained of persistent nausea, vomiting and weight loss had hypercalcemia and an elevated intact PTH level. Computed tomography confirmed two tumors in the thyroid gland. The tumors were surgically removed and pathologically confirmed as parathyroid adenoma. Because his maternal aunt and grandmother both had histories of parathyroid tumors, genetic investigation was undertaken for him, and a germline frameshift mutation of the CDC73 gene was identified. CDC73 gene analysis should be done on individuals who are at risk of familial hyperparathyroidism, including those who are asymptomatic, and they should be followed for potential primary hyperparathyroidism and associated disorders including resultant parathyroid carcinoma.
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来源期刊
Clinical Pediatric Endocrinology
Clinical Pediatric Endocrinology ENDOCRINOLOGY & METABOLISM-
CiteScore
2.40
自引率
7.10%
发文量
34
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