Levine Michael A, Germain-Lee Emily, Jan de Beur Suzanne
The Children's Hospital at The Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.
Horm Res. 2003;60 Suppl 3:87-95. doi: 10.1159/000074508.
Pseudohypoparathyroidism (PHP) is associated with biochemical hypoparathyroidism (i.e. hypocalcemia and hyperphosphatemia) due to parathyroid hormone (PTH) resistance rather than to PTH deficiency. Patients with PHP type 1a have a generalized form of hormone resistance plus a constellation of developmental defects termed Albright hereditary osteodystrophy (AHO). Within PHP type 1a families some individuals will show AHO but have normal hormone responsiveness, a variant phenotype termed pseudo-PHP. By contrast, patients with PHP type 1b manifest only PTH resistance and lack features of AHO. These various forms of PHP are due to defects in the GNAS1 gene that lead to decreased expression or activity of the alpha-subunit of the stimulatory G protein (G(s)alpha). Tissue-specific genomic imprinting of GNAS1 accounts for the variable phenotypes of patients with GNAS1 defects.
假性甲状旁腺功能减退症(PHP)与生化性甲状旁腺功能减退症(即低钙血症和高磷血症)相关,其病因是甲状旁腺激素(PTH)抵抗而非PTH缺乏。1a型PHP患者存在全身性激素抵抗以及一系列称为奥尔布赖特遗传性骨营养不良(AHO)的发育缺陷。在1a型PHP家族中,一些个体表现出AHO,但激素反应正常,这种变异表型称为假性PHP。相比之下,1b型PHP患者仅表现出PTH抵抗,且缺乏AHO的特征。这些不同形式的PHP是由GNAS1基因缺陷导致刺激性G蛋白(G(s)α)α亚基的表达或活性降低所致。GNAS1的组织特异性基因组印记解释了GNAS1缺陷患者的可变表型。