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首页> 外文期刊>Clinical Pediatric Endocrinology >An adolescent case of familial hyperparathyroidism with a germline frameshift mutation of the CDC73 gene
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An adolescent case of familial hyperparathyroidism with a germline frameshift mutation of the CDC73 gene

机译:伴有CDC73基因种系移码突变的家族性甲状旁腺功能亢进症青少年病例

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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.
机译:一名抱怨持续恶心,呕吐和体重减轻的13岁男孩患有高钙血症和完整PTH水平升高。计算机断层扫描证实了甲状腺中有两个肿瘤。手术切除肿瘤,并在病理上确认为甲状旁腺腺瘤。由于他的母亲姨母和祖母都有甲状旁腺肿瘤的病史,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。 CDC73基因分析应在具有家族性甲状旁腺功能亢进症风险的个体(包括无症状的个体)上进行,并应针对潜在的原发性甲状旁腺功能亢进症和相关疾病(包括导致的甲状旁腺癌)进行随访。

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