• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Absent intestinal response to calciferols in hereditary resistance to 1,25-dihydroxyvitamin D: documentation and effective therapy with high dose intravenous calcium infusions.

作者信息

Bliziotes M, Yergey A L, Nanes M S, Muenzer J, Begley M G, Vieira N E, Kher K K, Brandi M L, Marx S J

机构信息

Section on Mineral Metabolism, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland 20892.

出版信息

J Clin Endocrinol Metab. 1988 Feb;66(2):294-300. doi: 10.1210/jcem-66-2-294.

DOI:10.1210/jcem-66-2-294
PMID:2828407
Abstract

We describe a patient with an absent intestinal response to 1,25-dihydroxyvitamin D [1,25-(OH)2D] and the beneficial effects of treatment with high dose iv calcium infusion. The patient presented with severe rickets despite therapy with extraordinarily high doses of 1 alpha-hydroxyvitamin D3 or 1,25-(OH)2D3. Unidirectional intestinal fractional calcium absorption when he was not treated with any calciferol was 14% (normal, 20-70%), as measured with stable calcium isotopes; no increase in calcium absorption occurred when serum 1,25-(OH)2D levels were more than 50-fold elevated. Cultured skin fibroblasts contained no detectable 25-hydroxyvitamin D3-24-hydroxylase activity in response to 1,25-(OH)2D3 (10(-9)-10(-6) mol/L). High dose iv calcium infusions and oral phosphorus supplementation for 135 days improved or normalized biochemical parameters and resulted in radiographic healing of the rachitic lesions. We conclude that 1) this patient had no response to 1,25-(OH)2D3 in vivo and in vitro; 2) long term parenteral calcium infusions were effective therapy in managing the patient's severe resistance to 1,25-(OH)2D; and 3) stable calcium isotopes are useful for measuring low levels of fractional calcium absorption.

摘要

相似文献

1
Absent intestinal response to calciferols in hereditary resistance to 1,25-dihydroxyvitamin D: documentation and effective therapy with high dose intravenous calcium infusions.
J Clin Endocrinol Metab. 1988 Feb;66(2):294-300. doi: 10.1210/jcem-66-2-294.
2
Hereditary resistance to 1,25-dihydroxyvitamin D: clinical and radiological improvement during high-dose oral calcium therapy.遗传性1,25 - 二羟基维生素D抵抗:大剂量口服钙剂治疗期间的临床及影像学改善
Horm Res. 1986;24(4):280-7. doi: 10.1159/000180568.
3
Rickets and alopecia with resistance to 1,25-dihydroxyvitamin D: two different clinical courses with two different cellular defects.佝偻病与对1,25 - 二羟维生素D有抵抗的脱发症:两种不同的临床病程与两种不同的细胞缺陷。
J Clin Endocrinol Metab. 1983 Oct;57(4):803-11. doi: 10.1210/jcem-57-4-803.
4
The combined use of intravenous and oral calcium for the treatment of vitamin D dependent rickets type II (VDDRII).静脉注射与口服钙剂联合用于治疗II型维生素D依赖性佝偻病(VDDRII)。
Clin Endocrinol (Oxf). 1993 Aug;39(2):229-37. doi: 10.1111/j.1365-2265.1993.tb01779.x.
5
A new point mutation in the deoxyribonucleic acid-binding domain of the vitamin D receptor in a kindred with hereditary 1,25-dihydroxyvitamin D-resistant rickets.在一个患有遗传性1,25 - 二羟维生素D抵抗性佝偻病的家族中,维生素D受体的脱氧核糖核酸结合域出现一个新的点突变。
J Clin Endocrinol Metab. 1993 Feb;76(2):509-12. doi: 10.1210/jcem.76.2.8381803.
6
1alpha(OH)D3 One-alpha-hydroxy-cholecalciferol--an active vitamin D analog. Clinical studies on prophylaxis and treatment of secondary hyperparathyroidism in uremic patients on chronic dialysis.1α(OH)D3 一α-羟基胆钙化醇——一种活性维生素 D 类似物。关于慢性透析的尿毒症患者继发性甲状旁腺功能亢进症预防和治疗的临床研究。
Dan Med Bull. 2008 Nov;55(4):186-210.
7
Long-term nocturnal calcium infusions can cure rickets and promote normal mineralization in hereditary resistance to 1,25-dihydroxyvitamin D.长期夜间输注钙可治愈佝偻病,并促进对1,25 - 二羟维生素D具有遗传性抵抗的患者实现正常矿化。
J Clin Invest. 1986 May;77(5):1661-7. doi: 10.1172/JCI112483.
8
1 alpha-hydroxyvitamin D3 treatment of three patients with 1,25-dihydroxyvitamin D-receptor-defect rickets and alopecia.
Pediatrics. 1987 Jul;80(1):97-101.
9
Prenatal diagnosis of vitamin D-dependent rickets, type II: response to 1,25-dihydroxyvitamin D in amniotic fluid cells and fetal tissues.II型维生素D依赖性佝偻病的产前诊断:羊水细胞和胎儿组织对1,25-二羟维生素D的反应
J Clin Endocrinol Metab. 1990 Oct;71(4):937-43. doi: 10.1210/jcem-71-4-937.
10
Effect of 1,25-dihydroxyvitamin D3 treatment on bone formation by transplanted cells from normal and X-linked hypophosphatemic mice.1,25-二羟维生素D3治疗对正常和X连锁低磷血症小鼠移植细胞骨形成的影响。
J Bone Miner Res. 1995 Mar;10(3):424-31. doi: 10.1002/jbmr.5650100313.

引用本文的文献

1
Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese.中国遗传性维生素D抵抗性佝偻病中的新型维生素D受体突变
PLoS One. 2015 Sep 30;10(9):e0138152. doi: 10.1371/journal.pone.0138152. eCollection 2015.
2
Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets.维生素D受体突变与遗传性维生素D抵抗性佝偻病
Bonekey Rep. 2014 Mar 5;3:510. doi: 10.1038/bonekey.2014.5. eCollection 2014.
3
Vitamin D - Dependent Rickets, Type II Case Report.维生素D依赖性佝偻病,II型病例报告。
Mater Sociomed. 2014 Feb;26(1):68-70. doi: 10.5455/msm.2014.26.68-70. Epub 2014 Feb 20.
4
The role of vitamin D receptor mutations in the development of alopecia.维生素 D 受体突变在脱发中的作用。
Mol Cell Endocrinol. 2011 Dec 5;347(1-2):90-6. doi: 10.1016/j.mce.2011.05.045. Epub 2011 Jun 13.
5
Genetic disorders and defects in vitamin d action.遗传性疾病与维生素 D 作用缺陷。
Endocrinol Metab Clin North Am. 2010 Jun;39(2):333-46, table of contents. doi: 10.1016/j.ecl.2010.02.004.
6
Hereditary vitamin D resistant rickets: identification of a novel splice site mutation in the vitamin D receptor gene and successful treatment with oral calcium therapy.遗传性维生素D抵抗性佝偻病:维生素D受体基因新剪接位点突变的鉴定及口服钙剂治疗成功案例
Bone. 2009 Oct;45(4):743-6. doi: 10.1016/j.bone.2009.06.003. Epub 2009 Jun 10.
7
Hereditary vitamin D resistant rickets caused by a novel mutation in the vitamin D receptor that results in decreased affinity for hormone and cellular hyporesponsiveness.遗传性维生素D抵抗性佝偻病由维生素D受体的一种新突变引起,该突变导致对激素的亲和力降低和细胞低反应性。
J Clin Invest. 1997 Jan 15;99(2):297-304. doi: 10.1172/JCI119158.
8
Intra-atrial calcium infusions, growth, and development in end organ resistance to vitamin D.心房内钙输注、生长以及终末器官对维生素D的抵抗与发育
Arch Dis Child. 1993 Dec;69(6):689-92. doi: 10.1136/adc.69.6.689.
9
Selective expression of a normal action of the 1,25-dihydroxyvitamin D3 receptor in human skin fibroblasts with hereditary severe defects in multiple actions of that receptor.在具有该受体多种作用遗传性严重缺陷的人皮肤成纤维细胞中,1,25 - 二羟基维生素D3受体正常作用的选择性表达。
J Clin Invest. 1989 Jun;83(6):2093-101. doi: 10.1172/JCI114122.
10
The molecular basis of hereditary 1,25-dihydroxyvitamin D3 resistant rickets in seven related families.七个相关家族中遗传性1,25 - 二羟基维生素D3抵抗性佝偻病的分子基础。
J Clin Invest. 1990 Dec;86(6):2071-9. doi: 10.1172/JCI114944.