Sohár Nicolette, Jánossy Ágnes, Janáky Márta, Facskó Andrea
Szegedi Tudományegyetem, Szent-Györgyi Albert Orvos- és Gyógyszerésztudományi Centrum, Általános Orvostudományi Kar Szemészeti Klinika Szeged Korányi fasor 10-11. 6720.
Orv Hetil. 2013 Dec 29;154(52):2071-7. doi: 10.1556/OH.2013.29748.
Bardet-Biedl syndrome is characterised by retinal dystrophy, polydactily, obesity and slow mental development.
The aim of the authors was to present ophthalmologic signs and symptoms of the syndrome.
Between 1980 and 2010, 4 children with Bardet-Biedl syndrome were evaluated at the Department of Ophthalmology, University of Szeged, Szeged, Hungary. Their age at the first visit was between 1 and 10 years. Basic ophthalmological and electrophysiological evaluation, as well as orthoptic examinations were performed.
In two cases the electroretinographic curves were subnormal, and in two cases the electroretinographic curves showed no elevation. In the 4 children abnormal electroretinographic curves appeared at the ages of 1, 5, 10, and 18 years. Pigmentary changes on the periphery of the retina were detected in two cases.
The different signs and symptoms of Bardet-Biedl syndrome may manifest at different ages. Electrophysiological changes failed to correlate with retinal alterations is these patients.
巴德-比德尔综合征的特征为视网膜营养不良、多指(趾)畸形、肥胖及智力发育迟缓。
作者的目的是介绍该综合征的眼科体征和症状。
1980年至2010年间,匈牙利塞格德大学眼科对4例巴德-比德尔综合征患儿进行了评估。他们首次就诊时的年龄在1至10岁之间。进行了基本的眼科和电生理评估以及斜视检查。
2例视网膜电图曲线异常,2例视网膜电图曲线无升高。4例患儿分别在1岁、5岁、10岁和18岁时出现异常视网膜电图曲线。2例检测到视网膜周边色素改变。
巴德-比德尔综合征的不同体征和症状可能在不同年龄出现。在这些患者中,电生理变化与视网膜改变不相关。