先天性梨状孔鼻腔狭窄合并中枢性尿崩症。
Congenital nasal pyriform aperture stenosis associated with central diabetes insipidus.
作者信息
Godil M A, Galvin-Parton P, Monte D, Zerah M, Purandare A, Lane A H, Wilson T A
机构信息
Department of Pediatrics, State University of New York, Stony Brook 11794-8111, USA.
出版信息
J Pediatr. 2000 Aug;137(2):260-2. doi: 10.1067/mpd.2000.107187.
PMID:10931423
Abstract
We describe a child who has central diabetes insipidus associated with congenital nasal pyriform aperture stenosis without any apparent anterior pituitary dysfunction. This association further strengthens the concept that congenital nasal pyriform aperture stenosis may be a microform of holoprosencephaly.
摘要
我们描述了一名患有中枢性尿崩症并伴有先天性鼻梨状孔狭窄的儿童，且无任何明显的垂体前叶功能障碍。这种关联进一步强化了先天性鼻梨状孔狭窄可能是全前脑畸形一种微小型的概念。
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