Early presentation of pseudohypoparathyroidism.
作者信息
Hewitt M, Chambers T L
机构信息
Southmead Hospital, Westbury-on-Trym, Bristol.
出版信息
J R Soc Med. 1988 Nov;81(11):666-7. doi: 10.1177/014107688808101119.
Abstract
摘要
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引用本文的文献
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[Calcinosis cutis in Albright hereditary osteodystrophy: pseudohypoparathyroidism type Ia].[奥尔布赖特遗传性骨营养不良中的皮肤钙化：Ia型假性甲状旁腺功能减退症]
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Albright's hereditary osteodystrophy.奥尔布赖特遗传性骨营养不良症
J Med Genet. 1994 Oct;31(10):779-84. doi: 10.1136/jmg.31.10.779.
本文引用的文献
1
Albright's hereditary osteodystrophy comprising pseudohypoparathyroidism and pseudo-pseudohypoparathyroidism. With a report of two cases representing the complete syndrome occurring in successive generations.奥尔布赖特遗传性骨营养不良，包括假性甲状旁腺功能减退和假假性甲状旁腺功能减退。报告两例代表连续两代出现的完整综合征的病例。
Ann Intern Med. 1962 Feb;56:315-42. doi: 10.7326/0003-4819-56-2-315.
2
Pseudo-pseudohypoparathyroidism.假假性甲状旁腺功能减退症
Trans Assoc Am Physicians. 1952;65:337-50.
3
The development of pseudohypoparathyroidism. Involvement of progressively increasing serum parathyroid hormone concentrations, increased 1,25-dihydroxyvitamin D concentrations, and 'migratory' subcutaneous calcifications.假性甲状旁腺功能减退症的发展。血清甲状旁腺激素浓度逐渐升高、1,25 - 二羟维生素D浓度升高以及“游走性”皮下钙化的累及情况。
Am J Dis Child. 1984 Jul;138(7):654-8. doi: 10.1001/archpedi.1984.02140450036011.
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