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两兄弟患有类似口面指综合征II型和VI型的综合征且垂体缺失:一种新型口面指综合征?

Absent pituitary gland in two brothers with an oral-facial-digital syndrome resembling OFDS II and VI: a new type of OFDS?

作者信息

Shashi V, Clark P, Rogol A D, Wilson W G

机构信息

Department of Pediatrics, University of Virginia, Charlottesville 22908, USA.

出版信息

Am J Med Genet. 1995 May 22;57(1):22-6. doi: 10.1002/ajmg.1320570107.

Abstract

The oral-facial-digital syndromes (OFDS) comprise a group of heterogeneous genetic disorders. Considerable clinical overlap exists within the nine described types [Toriello, Clin Dysmorph 2:95-105, 1993], and with other entities such as Pallister-Hall (PH) syndrome and hydrolethalus syndrome, leading to difficulties in the classification of OFDS. We report on two brothers with findings overlapping OFDS II, VI, and Pallister-Hall syndrome who had congenital absence of the pituitary gland. This may represent a new type of OFDS or, alternatively, an example of phenotypic variability within the OFDS. It also emphasizes that agenesis of the pituitary gland can occur in a variety of syndromes with midline defects.

摘要

口面指综合征(OFDS)是一组具有异质性的遗传性疾病。在已描述的九种类型中存在相当多的临床重叠情况[Toriello,《临床畸形学》2:95 - 105,1993],并且与其他病症如帕利斯特 - 霍尔(PH)综合征和水致死性综合征也存在重叠,这导致了OFDS分类的困难。我们报告了两兄弟,他们具有与OFDS II型、VI型以及帕利斯特 - 霍尔综合征重叠的表现,且患有先天性垂体缺失。这可能代表一种新型的OFDS,或者是OFDS内表型变异的一个例子。它还强调垂体发育不全可发生于多种伴有中线缺陷的综合征中。

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