Verloes A, Dodinval P
Center for Human Genetics, Liège State University, Belgium.
Ophthalmic Paediatr Genet. 1990 Mar;11(1):41-7. doi: 10.3109/13816819009012948.
The authors report a girl with short stature, goniodysgenesis, bilateral iridochorio-retinal coloboma, associated with facial and acral anomalies, and borderline intelligence. Anterior chamber defect and face dysmorphism are in accordance with the diagnosis of Rieger syndrome. Some features are reminiscent of the CHARGE association. Coloboma, abnormal ears, grooved palate, elbow pronosupination and hand bones anomalies are related to the Abruzzo-Erikson syndrome. The authors postulate that their propositus may represent a new occurrence of the latter syndrome, and they propose to widen the actual definition of Abruzzo-Erikson syndrome to the association of goniodysgenesis, coloboma, abnormal ears and upper limb anomalies.
作者报告了一名身材矮小、前房角发育不全、双侧虹膜脉络膜视网膜缺损,并伴有面部和肢体末端异常以及边缘智力的女孩。前房缺损和面部畸形符合里格尔综合征的诊断。一些特征使人联想到CHARGE综合征。缺损、耳部异常、腭裂、肘部旋前旋后和手部骨骼异常与阿布鲁佐 - 埃里克森综合征有关。作者推测他们的先证者可能代表了后者综合征的一种新出现情况,并建议将阿布鲁佐 - 埃里克森综合征的现有定义扩大到包括前房角发育不全、缺损、耳部异常和上肢异常的关联。