Pang Qianqian, Qi Xuan, Jiang Yan, Wang Ou, Li Mei, Xing Xiaoping, Dong Jin, Xia Weibo
Department of Endocrinology, Key Laboratory of Endocrinology, The Ministry of Health, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China; Department of Endocrinology, The First Affiliated Hospital of Shanxi Medical University, Taiyuan, China.
Department of Endocrinology, Key Laboratory of Endocrinology, The Ministry of Health, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences , Beijing, China.
Bone Res. 2016 Jun 21;4:16018. doi: 10.1038/boneres.2016.18. eCollection 2016.
Hereditary vitamin D-resistant rickets (HVDRR) is a rare autosomal recessive disorder characterized by severe rickets, hypocalcemia, hypophosphatemia, secondary hyperparathyroidism, and elevated alkaline phosphatase. This disorder is caused by homogeneous or heterogeneous mutations affecting the function of the vitamin D receptor (VDR), which lead to complete or partial target organ resistance to the action of 1,25-dihydroxy vitamin D. A non-consanguineous family of Chinese Han origin with one affected individual demonstrating HVDRR was recruited, with the proband evaluated clinically, biochemically and radiographically. To identify the presence of mutations in the VDR gene, all the exons and exon-intron junctions of the VDR gene from all family members were amplified using PCR and sequenced. The proband showed rickets, progressive alopecia, hypocalcemia, hypophosphatemia, secondary hyperparathyroidism, and elevated alkaline phosphatase. She also suffered from epilepsy, which is rarely seen in patients with HVDRR. Direct sequencing analysis revealed a homozygous missense mutation c.122G>A (p.C41Y) in the VDR gene of the proband, which is located in the first zinc finger of the DNA-binding domain. Both parents had a normal phenotype and were found to be heterozygous for this mutation. We report a Chinese Han family with one individual affected with HVDRR. A homozygous missense mutation c.122G>A (p.C41Y) in the VDR gene was found to be responsible for the patient's syndrome. In contrast to the results of treatment of HVDRR in other patients, our patient responded well to a supplement of oral calcium and a low dose of calcitriol.
遗传性维生素D抵抗性佝偻病(HVDRR)是一种罕见的常染色体隐性疾病,其特征为严重佝偻病、低钙血症、低磷血症、继发性甲状旁腺功能亢进以及碱性磷酸酶升高。这种疾病由影响维生素D受体(VDR)功能的纯合或杂合突变引起,导致靶器官对1,25 - 二羟维生素D的作用产生完全或部分抵抗。招募了一个中国汉族非近亲家庭,该家庭中有一名个体表现出HVDRR,对先证者进行了临床、生化和影像学评估。为了确定VDR基因中是否存在突变,使用聚合酶链反应(PCR)扩增了所有家庭成员VDR基因的所有外显子和外显子 - 内含子连接区并进行测序。先证者表现出佝偻病、进行性脱发、低钙血症、低磷血症、继发性甲状旁腺功能亢进以及碱性磷酸酶升高。她还患有癫痫,这在HVDRR患者中很少见。直接测序分析显示先证者的VDR基因存在纯合错义突变c.122G>A(p.C41Y),该突变位于DNA结合域的第一个锌指中。父母双方表型正常,且被发现为该突变的杂合子。我们报告了一个中国汉族家庭,其中一名个体患有HVDRR。发现VDR基因中的纯合错义突变c.122G>A(p.C41Y)是导致该患者综合征的原因。与其他HVDRR患者的治疗结果不同,我们的患者对口服补钙和低剂量骨化三醇补充剂反应良好。