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原发性甲状旁腺功能亢进症与奥尔布赖特遗传性骨营养不良并存——一种不寻常的关联。

Coexisting primary hyperparathyroidism and Albright's hereditary osteodystrophy--an unusual association.

作者信息

Sasaki H, Tsutsu N, Asano T, Yamamoto T, Kikuchi M, Okumura M

出版信息

Postgrad Med J. 1985 Feb;61(712):153-5. doi: 10.1136/pgmj.61.712.153.

DOI:10.1136/pgmj.61.712.153
PMID:3983044
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2418159/
Abstract

Primary hyperparathyroidism associated with Albright's hereditary osteodystrophy was diagnosed in a 22 year old Japanese woman, the second such case to be reported. Albright's hereditary osteodystrophy (AHO) appears to be associated with a larger number of disorders than the well recognized pseudohypoparathyroidism. AHO and pseudo-pseudohypoparathyroidism are essentially identical.

摘要

一名22岁的日本女性被诊断出患有与奥尔布赖特遗传性骨营养不良相关的原发性甲状旁腺功能亢进症,这是第二例此类病例报告。与广为人知的假性甲状旁腺功能减退症相比,奥尔布赖特遗传性骨营养不良(AHO)似乎与更多的疾病有关。AHO和假性假性甲状旁腺功能减退症本质上是相同的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5377/2418159/8968ea7edefa/postmedj00108-0062-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5377/2418159/8968ea7edefa/postmedj00108-0062-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5377/2418159/8968ea7edefa/postmedj00108-0062-a.jpg

相似文献

1
Coexisting primary hyperparathyroidism and Albright's hereditary osteodystrophy--an unusual association.原发性甲状旁腺功能亢进症与奥尔布赖特遗传性骨营养不良并存——一种不寻常的关联。
Postgrad Med J. 1985 Feb;61(712):153-5. doi: 10.1136/pgmj.61.712.153.
2
Spinal Stenosis with Paraparesis in a Korean Boy with Albright's Hereditary Osteodystrophy: Identification of a Novel Nonsense Mutation in the GNAS.一名患有奥尔布赖特遗传性骨营养不良的韩国男孩出现伴有轻截瘫的脊髓狭窄:GNAS基因中一个新的无义突变的鉴定
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Cutaneous ossification in Albright's hereditary osteodystrophy.奥尔布赖特遗传性骨营养不良中的皮肤骨化
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Pseudohypoparathyroidism with Albright's hereditary osteodystrophy (AHO) phenotype.伴有奥尔布赖特遗传性骨营养不良(AHO)表型的假性甲状旁腺功能减退症。
J Assoc Physicians India. 2004 Jan;52:46.
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Parental origin of Gs alpha gene mutations in Albright's hereditary osteodystrophy.奥尔布赖特遗传性骨营养不良中Gsα基因突变的亲本来源
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Imprinting in Albright's hereditary osteodystrophy.奥尔布赖特遗传性骨营养不良中的印记现象。
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Pseudohypoparathyroidism type I and Albright's hereditary osteodystrophy with a proximal 15q chromosomal deletion in mother and daughter.母女患有 I 型假性甲状旁腺功能减退症及伴有近端 15q 染色体缺失的奥尔布赖特遗传性骨营养不良症。
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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
Calcification of the basal ganglia of the brain.脑基底神经节钙化。
Am J Roentgenol Radium Ther Nucl Med. 1959 Nov;82:806-22.
3
Pseudo-pseudohypoparathyroidism.
假假性甲状旁腺功能减退症
Trans Assoc Am Physicians. 1952;65:337-50.
4
Albright's hereditary osteodystrophy: a review.奥尔布赖特遗传性骨营养不良症综述
Am J Med Genet. 1982 Jan;11(1):11-29. doi: 10.1002/ajmg.1320110104.
5
Familial pseudohypoparathyroidism without somatic anomalies.无躯体异常的家族性假性甲状旁腺功能减退症。
Can Med Assoc J. 1980 Jul 5;123(1):26-31.
6
Hyperparathyroidism with Albright's osteodystrophy: Case report and a proposed new classification of parathyroid disease.甲状旁腺功能亢进伴奥尔布赖特骨营养不良:病例报告及甲状旁腺疾病新分类建议
J Clin Endocrinol Metab. 1970 Sep;31(3):271-6. doi: 10.1210/jcem-31-3-271.
7
Parathyroid hormone deficiency with Albright's hereditary osteodystrophy.甲状旁腺激素缺乏伴奥尔布赖特遗传性骨营养不良。
J Clin Endocrinol Metab. 1974 Sep;39(3):496-500. doi: 10.1210/jcem-39-3-496.
8
The spectrum of the hypoparathyroid states: A classification based on physiologic principles.甲状旁腺功能减退状态的谱系:基于生理原理的分类。
Medicine (Baltimore). 1976 Mar;55(2):105-19. doi: 10.1097/00005792-197603000-00001.