Suppr超能文献

Occurrences of methylmalonic aciduria and Hartnup disorder in the same family.

作者信息

Shih V E, Coulombe J T, Wadman S K, Duran M, Waelkens J J

出版信息

Clin Genet. 1984 Sep;26(3):216-20. doi: 10.1111/j.1399-0004.1984.tb04370.x.

Abstract

Methylmalonic aciduria and Hartnup disorder are two rare autosomal recessively inherited metabolic disorders. We have described the coexistence of these disorders within the same pedigree in two unrelated families. This association was not found in 57 other families surveyed because of a proband known to have either methylmalonic aciduria or Hartnup disorder.

摘要

相似文献

1
Occurrences of methylmalonic aciduria and Hartnup disorder in the same family.
Clin Genet. 1984 Sep;26(3):216-20. doi: 10.1111/j.1399-0004.1984.tb04370.x.
3
B12-unresponsive methylmalonic aciduria in a female infant.
J Inherit Metab Dis. 1980;3(3):91-2. doi: 10.1007/BF02312536.
5
Methylmalonic aciduria (1 case report).甲基丙二酸尿症(1例报告)
Proc Chin Acad Med Sci Peking Union Med Coll. 1987;2(3):183-5.
6
[Methylmalonic aciduria].[甲基丙二酸尿症]
Nihon Rinsho. 1978 May;Suppl:1362-3.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验