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Beyond Gómez-López-Hernández Syndrome: Recurring Phenotypic Themes in Rhombencephalosynapsis

机译:除了Gómez-lópez-hernández综合征:refurring在rhombencephalosynapsis中的表型主题

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摘要

Rhombencephalosynapsis (RES) is an uncommon cerebellar malformation characterized by fusion of the hemispheres without an intervening vermis. Frequently described in association with Gómez-López-Hernández syndrome, RES also occurs in conjunction with VACTERL features and with holoprosencephaly (HPE). We sought to determine the full phenotypic spectrum of RES in a large cohort of patients. Information was obtained through database review, patient questionnaire, radiographic and morphologic assessment, and statistical analysis. We assessed 53 patients. 33 had alopecia, 3 had trigeminal anesthesia, 14 had VACTERL features and 2 had HPE with aventriculy. Specific craniofacial features were seen throughout the cohort, but were more common in patients with alopecia. We noted substantial overlap between groups. We conclude that although some distinct subgroups can be delineated, the overlapping features seen in our cohort suggest an underlying spectrum of RES-associated malformations rather than a collection of discrete syndromes.
机译:菱形脑突触(RES)是一种不常见的小脑畸形,其特征是半球融合而无ver骨。 RES通常与Gómez-López-Hernández综合征相关联描述,也与VACTERL功能和全前脑(HPE)一起出现。我们试图确定一大群患者中RES的完整表型谱。通过数据库审查,患者问卷,影像学和形态学评估以及统计分析获得信息。我们评估了53名患者。脱发33例,三叉神经阻滞3例,VACTERL征象14例,HPE伴室颤。在整个队列中均可见特定的颅面特征,但在脱发患者中更为常见。我们注意到组之间存在大量重叠。我们得出的结论是,尽管可以描绘出一些不同的亚组,但在我们的队列中看到的重叠特征表明与RES相关的畸形存在潜在的频谱,而不是离散综合症的集合。

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