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常染色体隐性遗传性特发性纹状体-苍白球-齿状核钙化症和科凯恩综合征中的钙磷代谢

Calcium-phosphate metabolism in autosomal recessive idiopathic strio-pallido-dentate calcinosis and Cockayne's syndrome.

作者信息

Smits M G, Gabreëls F J, Froeling P G, de Abreu R A, Thijssen H O, Renier W O

出版信息

Clin Neurol Neurosurg. 1983;85(3):145-53. doi: 10.1016/0303-8467(83)90044-6.

Abstract

In three siblings with autosomal recessive idiopathic strio-pallido-dentate calcinosis (SPDC) and in three other siblings with Cockayne's syndrome (CS) studies on plasma values of calcium and phosphate, intestinal calcium absorption, radiograms of the hands and studies on the influence of parathyroid hormone (PTH) on the renal threshold for phosphate revealed no abnormalities. In one of the SPDC patients and one of the CS patients the effect of PTH on the cyclic adenosine monophosphate (cAMP) concentrations in urine and cerebrospinal fluid (CSF) were determined. In both a normal response of urinary cAMP was noted. In the CS patient the response of CSF cAMP was also normal. The SPDC patient, however, had a significantly decreased response of CSF cAMP. It is suggested that a decreased sensitivity of the cerebral adenylate cyclase complex is involved in the etiology of autosomal recessive idiopathic SPDC. Subsequently this disorder could be considered as cerebral pseudohypoparathyroidism. The etiology of CS remains unknown.

摘要

在3例患有常染色体隐性遗传性特发性纹状体 - 苍白球 - 齿状核钙化症(SPDC)的同胞以及3例患有科凯恩综合征(CS)的其他同胞中,对血钙和血磷水平、肠道钙吸收、手部X光片以及甲状旁腺激素(PTH)对肾磷酸盐阈值的影响进行的研究均未发现异常。在1例SPDC患者和1例CS患者中,测定了PTH对尿液和脑脊液(CSF)中环状单磷酸腺苷(cAMP)浓度的影响。在两者中均观察到尿cAMP的正常反应。在CS患者中,CSF cAMP的反应也正常。然而,SPDC患者的CSF cAMP反应明显降低。提示大脑腺苷酸环化酶复合物敏感性降低与常染色体隐性遗传性特发性SPDC的病因有关。随后,这种疾病可被视为脑假性甲状旁腺功能减退症。CS的病因仍然未知。

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