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新生儿肾上腺脑白质营养不良中的高哌可酸血症

Hyperpipecolic acidemia in neonatal adrenoleukodystrophy.

作者信息

Kelley R I, Moser H W

出版信息

Am J Med Genet. 1984 Dec;19(4):791-5. doi: 10.1002/ajmg.1320190420.

Abstract

Serum pipecolic acid was measured in patients with neonatal adrenoleukodystrophy (NALD), sex-linked ALD, and the cerebrohepatorenal syndrome of Zellweger. Pipecolic acid was elevated, often markedly, in most of the patients with NALD but in none of those with X-linked ALD or adrenomyeloneuropathy, or in normal adults and children, or children with cirrhosis or other neurodegenerative disorders. The demonstration of elevated serum pipecolic acid in NALD adds to the previously recognized elevation of very-long-chain fatty acids (another Zellweger syndrome sign) and suggests that generalized peroxisomal dysfunction may be a characteristic of NALD as it appears to be of Zellweger syndrome, which diseases share some clinical characteristics. The nosologic significance of these findings is discussed.

摘要

对患有新生儿肾上腺脑白质营养不良(NALD)、X连锁肾上腺脑白质营养不良(ALD)以及齐韦格脑肝肾综合征的患者测定了血清哌可酸。大多数NALD患者的哌可酸升高,且常常显著升高,但X连锁ALD或肾上腺脊髓神经病患者、正常成人和儿童、患有肝硬化或其他神经退行性疾病的儿童均未出现这种情况。NALD患者血清哌可酸升高的发现,进一步证明了之前已确认的极长链脂肪酸升高(另一个齐韦格综合征体征),并提示全身性过氧化物酶体功能障碍可能是NALD的一个特征,就如同它是齐韦格综合征的特征一样,这两种疾病有一些共同的临床特征。本文讨论了这些发现的疾病分类学意义。

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