在遗传性原发性甲状腺功能障碍症中临床表型和遗传查:一个单中心病例系列
Gu Yian1, Yuanyuan Ye1, Xu Ning1
1Department of Endocrinology and Metabolism, Tianjin Medical University General Hospital, Tianjin, China.
Annales d'endocrinologie
|May 18, 2025
概括
遗传性原发性甲状腺功能障碍症 (PHPT) 是罕见的,但这项研究详细介绍了其遗传原因和中国的临床特征. 基因检测对于诊断PHPT亚型和指导治疗至关重要.
科学领域:
- 内分泌学 在内分泌学.
- 遗传学 遗传学 是一个
- 在瘤学瘤学.
背景情况:
- 遗传性原发性甲状腺功能障碍 (PHPT) 是一种罕见的遗传性疾病,影响5-10%的PHPT病例.
- 在中国人群中遗传性PHPT的数据有限.
研究的目的:
- 描述中国遗传性PHPT的病因,表型,基因型,管理和预后.
- 扩大已知的致病基因谱和评估年龄依赖的透性.
- 探索多发性内分泌新生病1型 (MEN1) 中的基因型-表型相关性.
主要方法:
- 追溯分析73名患者的医疗记录 (2008-2024年).
- 包括临床表现,生物化学标记,成像和整个外基因组测序.
- 在57名患者中发现了12种新突变.
主要成果:
- 多重内分泌瘤1型 (MEN1) 是最常见的原因 (80.8%).
- 在70.2%的受试患者中发现了致病变体.
- 呈现的平均年龄为42.0±14.5岁,在45岁时64.3%的透率.
结论:
- 基因检测对于分类遗传性PHPT亚型,监测并发症和指导治疗至关重要.
- 推用于患有早期发病,复杂表现,多腺体干扰或家族病史的患者.
- 强调基因测试对于遗传性PHPT的管理和监测的重要性.
相关概念视频
The Parathyroid Glands
The two pairs of parathyroid glands embedded within the posterior surface of the thyroid gland are restricted by a dense capsule around them. These glands comprise two distinct cell populations—parathyroid oxyphil and parathyroid principal cells- pivotal in calcium homeostasis.
Oxyphil cells, whose functions remain elusive, emerge during late puberty, adding a layer of complexity to the parathyroid gland's intricacies. In contrast, principal parathyroid cells undertake a vital role by producing...
Oxyphil cells, whose functions remain elusive, emerge during late puberty, adding a layer of complexity to the parathyroid gland's intricacies. In contrast, principal parathyroid cells undertake a vital role by producing...
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
Hyperthyroidism I: Introduction
Hyperthyroidism is a type of thyrotoxicosis characterized by the thyroid gland's overproduction of the thyroid hormones triiodothyronine (T3) and thyroxine (T4). This hormone excess increases the basal metabolic rate and enhances sensitivity to catecholamines.DiagnosisDiagnosis is based on clinical features and biochemical testing. It typically shows suppressed thyroid-stimulating hormone (TSH) levels below 0.4 mIU/L, with elevated free T3 and/or T4. Additional tests, including thyroid...
Hyperthyroidism II: Pathophysiology
Hyperthyroidism is a hypermetabolic state caused by elevated levels of thyroid hormones, triiodothyronine (T3) and thyroxine (T4). It results from dysregulation at the thyroid, pituitary, or immune system level and affects multiple organ systems.PathophysiologyThe most common cause of hyperthyroidism is Graves’ disease, an autoimmune disorder in which antibodies, specifically thyroid-stimulating antibodies (TSAb), a subtype of TSH receptor antibodies (TRAb), bind to and activate TSH receptors...
Graves Disease II: Pathophysiology
Graves’ disease is an autoimmune disorder characterized by the production of thyroid-stimulating immunoglobulins (TSI) that activate TSH receptors, leading to excessive synthesis and release of thyroid hormones (T3 and T4) and resulting in hyperthyroidism.Among all causes of hyperthyroidism, Graves’ disease is the most common and can happen at any age, though it is more frequent in women. It produces a hypermetabolic state with features such as weight loss, tachycardia, tremor, and heat...


