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Father to son transmission of decreased Ns activity in pseudohypoparathyroidism type Ia.

作者信息

Van Dop C, Bourne H R, Neer R M

出版信息

J Clin Endocrinol Metab. 1984 Nov;59(5):825-8. doi: 10.1210/jcem-59-5-825.

DOI:10.1210/jcem-59-5-825
PMID:6090498
Abstract

We found both renal resistance to endogenous and exogenous PTH and reduced activity of the stimulatory guanine nucleotide-binding regulatory protein (Ns) of adenylate cyclase in a man with clinical signs of pseudohypoparathyroidism type Ia (PHP-Ia). Both of his children also had reduced Ns levels and short stature. The girl, 11 yr old, had evidence of partial resistance to PTH, while the son, age 7 yr, had no apparent abnormalities in calcium metabolism or response to administered PTH. Variable expression of the metabolic abnormalities of PHP during childhood has been previously described. The occurrence of reduced Ns activity in father and son is consistent with autosomal dominant inheritance for the primary biochemical defect of PHP-Ia in this family.

摘要

相似文献

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Father to son transmission of decreased Ns activity in pseudohypoparathyroidism type Ia.
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2
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引用本文的文献

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Rev Endocr Metab Disord. 2000 Nov;1(4):265-74. doi: 10.1023/a:1026510200264.
2
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。
J Med Genet. 1993 Feb;30(2):101-3. doi: 10.1136/jmg.30.2.101.
3
Genetic deficiency of the alpha subunit of the guanine nucleotide-binding protein Gs as the molecular basis for Albright hereditary osteodystrophy.鸟嘌呤核苷酸结合蛋白Gs的α亚基基因缺陷是奥尔布赖特遗传性骨营养不良的分子基础。
Proc Natl Acad Sci U S A. 1988 Jan;85(2):617-21. doi: 10.1073/pnas.85.2.617.