Okten A, Mungan L, Orhan F, Cakir M
Department of Pediatrics, Faculty of Medicine Karadeniz Technical University, Trabzon, Turkey.
Genet Couns. 2005;16(1):101-5.
We describe a newborn with multiple congenital anomalies consistent with an oro-facio-digital syndrome (OFDS). These are a group of inherited syndromes that have in common anomalies of the tongue (bifid or lobulated tongue with hamartomas), the face (median cleft lip) and the digits (brachydactyly, polydactyly, clinodactyly and/or syndactyly). OFDS has been classified into 11 types. The case described in this paper had manifestations overlapping with OFDS II (Mohr) and OFDS IV (Mohr-Majewski) and OFDS VI (Varadi). We propose that the present patient has a new variation of the OFDS due to the co-existence of the very atypical combination of polydactyly, cerebellar hypoplasia, hypothalamic hamartoma and classical facial findings of OFDS.
我们描述了一名患有多种先天性异常的新生儿,这些异常与口面指综合征(OFDS)相符。这是一组遗传性综合征,其共同特征为舌部异常(伴有错构瘤的分叉或分叶舌)、面部异常(正中唇裂)和手指异常(短指、多指、弯指和/或并指)。OFDS已被分为11种类型。本文所描述的病例表现与OFDS II型(莫尔型)、OFDS IV型(莫尔-马耶夫斯基型)和OFDS VI型(瓦拉迪型)重叠。我们认为,由于该患者同时存在多指、小脑发育不全、下丘脑错构瘤以及OFDS典型面部表现这种非常不典型的组合,因此其患有OFDS的一种新变异型。