• 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

[A case of pseudohypoparathyroidism coexisting with primary hypothyroidism and low bone mineral density in relation to age].

作者信息

Zatońska Katarzyna, Bolanowski Marek, Bednarek-Tupikowska Grazyna

机构信息

Katedra i Klinika Endokrynologii i Diabetologii Akademii Medycznej im. Piastów Slaskich we Wrocławiu.

出版信息

Pol Merkur Lekarski. 2002 Mar;12(69):235-7.

PMID:12053597
Abstract

We report a case of 18 year old woman with pseudohypoparathyroidism type la presenting with low bone mineral density and primary hypothyroidism. The patient was diagnosed because of muscular cramps, accompanied by elevated parathormone (PTH) level and hypocalciuria, but normal serum calcium, phosphate and magnesium levels. She had features of Albright's osteodystrophy: short stature with normal bone age, shortening of IV and V metacarpal bones, and small cerebral calcifications shown by CT.

摘要

相似文献

1
[A case of pseudohypoparathyroidism coexisting with primary hypothyroidism and low bone mineral density in relation to age].
Pol Merkur Lekarski. 2002 Mar;12(69):235-7.
2
Early manifestation of obesity and calcinosis cutis in infantile pseudohypoparathyroidism.婴儿假性甲状旁腺功能减退症中肥胖和皮肤钙化的早期表现。
J Paediatr Child Health. 2006 Dec;42(12):821-3. doi: 10.1111/j.1440-1754.2006.00985.x.
3
Pseudohypoparathyroidism-Albright hereditary osteodystrophy.
Indian J Pediatr. 1998 May-Jun;65(3):477-80. doi: 10.1007/BF02761150.
4
Early manifestation of calcinosis cutis in pseudohypoparathyroidism type Ia associated with a novel mutation in the GNAS gene.Ia型假性甲状旁腺功能减退症中皮肤钙化的早期表现与GNAS基因的一种新突变相关。
Eur J Endocrinol. 2005 Apr;152(4):515-9. doi: 10.1530/eje.1.01879.
5
[A case of pseudohypoparathyroidism].[一例假性甲状旁腺功能减退症病例]
Przegl Lek. 1999;56(11):743-6.
6
Intracranial calcification and brachydactyly mimicking Albright's hereditary osteodystrophy in an adult patient with lingual thyroid and prolactinoma-like lesion.一名患有舌甲状腺和催乳素瘤样病变的成年患者出现颅内钙化和短指畸形，酷似奥尔布赖特遗传性骨营养不良。
J Formos Med Assoc. 1991 Feb;90(2):189-94.
7
Albright's hereditary osteodystrophy.奥尔布赖特遗传性骨营养不良症
J Pediatr Endocrinol Metab. 2006 May;19 Suppl 2:671-3. doi: 10.1515/jpem.2006.19.s2.671.
8
[Albright's hereditary osteodystrophy: report of three cases].[奥尔布赖特遗传性骨营养不良：三例报告]
Arch Argent Pediatr. 2010 Apr;108(2):e24-7. doi: 10.1590/S0325-00752010000200012.
9
[Extensive intracerebral calcifications in a patient with pseudohypoparathyroidism (Albright syndrome)].[假性甲状旁腺功能减退症（奥尔布赖特综合征）患者的广泛脑内钙化]
Neurol Neurochir Pol. 2002 Mar-Apr;36(2):377-83.
10
[Primary hypothyroidism revealing pseudohypoparathyroidism without hypocalcemia and hyperphosphoremia].
Arch Pediatr. 1997 May;4(5):433-7. doi: 10.1016/s0929-693x(97)86669-9.