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家族性X连锁肾上腺皮质功能减退症作为肾上腺脑白质营养不良(ALD)的一种表现:培养的皮肤成纤维细胞中C26脂肪酸升高。

Familial X-linked Addison disease as an expression of adrenoleukodystrophy (ALD): elevated C26 fatty acid in cultured skin fibroblasts.

作者信息

O'Neill B P, Moser H W, Saxena K M

出版信息

Neurology. 1982 May;32(5):543-7. doi: 10.1212/wnl.32.5.543.

Abstract

Adrenoleukodystrophy (ALD) is a fatal X-linked disorder of very long chain fatty acid (VLCFA) metabolism manifested by disease of the central and peripheral nervous systems and the adrenals. X-linked Addison disease alone, as an expression of ALD, has not been previously reported. We present the results of our study of a unique family among whom clinically apparent Addison disease without neurologic involvement has occurred in affected males, and spastic paraparesis has occurred in female carriers. The presence of ALD was confirmed by VLCFA determination in cultured skin fibroblasts. A comparison group of patients with Addison disease on a putative immunopathogenic basis was normal.

摘要

肾上腺脑白质营养不良(ALD)是一种致命的X连锁极长链脂肪酸(VLCFA)代谢紊乱疾病,表现为中枢和周围神经系统以及肾上腺疾病。单独作为ALD表现形式的X连锁艾迪生病以前未见报道。我们报告了对一个独特家族的研究结果,在该家族中,受影响男性出现了无神经系统受累的临床明显艾迪生病,女性携带者出现了痉挛性截瘫。通过测定培养的皮肤成纤维细胞中的VLCFA证实了ALD的存在。一组基于推测的免疫致病基础的艾迪生病患者作为对照组结果正常。

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