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[Albright's type II osteodystrophy and hypothyroidism due to TSH deficiency. Apropos of a case in a child].

作者信息

David M, Madjar J J, Floret D, Sann L, Terrier M, Jeune M

出版信息

Arch Fr Pediatr. 1977 Feb;34(2):108-29.

PMID:194544
Abstract

The report is dealing with a 10 year-old girl. The diagnosis of Albright's type II osteodystrophy relied on clinical, radiological and biological symptoms: evocative dysmorphic syndrome and absence of disturbances in the phosphocalcic metabolism. Hypothyroidism was secondary to an isolated defect in TSH, and a TRH stimulation test did not induce an increase in plasma TSH.

摘要

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1
[Albright's type II osteodystrophy and hypothyroidism due to TSH deficiency. Apropos of a case in a child].
Arch Fr Pediatr. 1977 Feb;34(2):108-29.
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Albright's hereditary osteodystrophy: a review.奥尔布赖特遗传性骨营养不良症综述
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Pseudohypoparathyroidism: inheritance and expression of deficient receptor-cyclase coupling protein activity.假性甲状旁腺功能减退症:受体 - 环化酶偶联蛋白活性缺乏的遗传与表达
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Activity of the stimulatory guanine nucleotide-binding protein is reduced in erythrocytes from patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism: biochemical, endocrine, and genetic analysis of Albright's hereditary osteodystrophy in six kindreds.假性甲状旁腺功能减退症和假假性甲状旁腺功能减退症患者红细胞中刺激性鸟嘌呤核苷酸结合蛋白的活性降低:六个家系中奥尔布赖特遗传性骨营养不良的生化、内分泌和遗传学分析
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[Cutaneous osteoma and Albright's hereditary osteodystrophy].[皮肤骨瘤与奥尔布赖特遗传性骨营养不良]
Ann Dermatol Venereol. 1994;121(5):408-13.

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