A rare case of pseudohypoparathyroidism

V. Gubkina, T. Kamynina, E. Kornilova, A. Dreval
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Abstract

Pseudohypoparathyroidism (PGPT) - Albright's hereditary osteodystrophy is a sex-related disease rarely seen in medical practice. Inherited by the dominant type. It is caused by insensitivity of the kidneys and bones to parathyroid hormone (PG), which is secreted in normal or slightly elevated amounts [6, 10]. GH may not have a specific effect on cells due to pathology of GH receptors, impaired expression of information RNA synthesis by an unchanged hormone-receptor complex, the presence of pathological components of adenylate cyclase, pathological AMP-dependent protein kinase, or a defect in the synthesis of kinase substrates in the presence of circulating GH antagonists [5, 10 ].
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假性甲状旁腺功能减退1例
假性甲状旁腺功能减退症(PGPT) - Albright's遗传性骨营养不良症是一种罕见的与性别有关的疾病。由显性遗传的。它是由肾脏和骨骼对甲状旁腺激素(PG)不敏感引起的,PG的分泌量正常或略高[6,10]。由于生长激素受体的病理、未改变的激素受体复合物导致信息RNA合成表达受损、腺苷酸环化酶的病理成分、病理性amp依赖性蛋白激酶的存在,或者循环生长激素拮抗剂存在时激酶底物合成缺陷,生长激素可能对细胞没有特异性作用[5,10]。
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