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阿尔斯特伦综合征。22例报告及文献综述。

Alström syndrome. Report of 22 cases and literature review.

作者信息

Russell-Eggitt I M, Clayton P T, Coffey R, Kriss A, Taylor D S, Taylor J F

机构信息

Great Ormond Street Hospital for Children, London, England.

出版信息

Ophthalmology. 1998 Jul;105(7):1274-80. doi: 10.1016/S0161-6420(98)97033-6.

Abstract

OBJECTIVE

The authors report 22 cases of Alström syndrome (AS), which is the largest series to date. Only 37 cases have been reported in the world literature since 1959. The authors review the clinical features and compare these with the overlapping condition of Bardet-Biedl syndrome. Their aim is to clarify the AS phenotype and to increase awareness of the early features.

DESIGN

A retrospective case series.

PARTICIPANTS

All patients (22) with a diagnosis of AS admitted to the authors' hospital in the past 10 years were included in this review.

INTERVENTION

This is principally a review of ocular features, but other features are recorded and discussed.

MAIN OUTCOME MEASURES

Features noted included age at onset of visual symptoms, presence of photophobia, visual acuity, and electroretinogram findings. Nonocular features recorded included cardiac status, weight and height, hearing, and presence of diabetes mellitus.

RESULTS

Cardiomyopathy presenting in infancy has only been recognized recently to be a feature of AS. Of the authors' cases, 18 of 22 had infantile cardiomyopathy. In the authors' tertiary referral institution, there is an ascertainment bias toward younger patients and especially those with pathology that is other than ocular pathology. In addition, AS is difficult to recognize in childhood without the development of infantile cardiomyopathy. Alström syndrome often is not recognized until diabetes mellitus develops in the second or third decade. Initially, a diagnosis of cone-rod dystrophy, achromatopsia, Leber's congenital amaurosis, or Bardet-Biedl syndrome may be made. In AS, there is a severe infantile retinal dystrophy. The electroretinogram is absent or attenuated with better preserved rod than cone function. The retinal dystrophy is progressive with the patient's visual acuity of 6/60 or less by 10 years of age and no light perception by 20 years of age.

CONCLUSIONS

A diagnosis of AS should be considered in infantile cone and rod retinal dystrophy, particularly if the weight is above the 90th percentile (16 of 18 cases) or if there is an infantile cardiomyopathy (18 of 22 cases).

摘要

目的

作者报告了22例阿尔斯特伦综合征(AS)病例,这是迄今为止最大的病例系列。自1959年以来,世界文献中仅报道了37例。作者回顾了其临床特征,并将这些特征与巴德-比德尔综合征的重叠情况进行比较。他们的目的是阐明AS的表型,并提高对早期特征的认识。

设计

一项回顾性病例系列研究。

参与者

本综述纳入了过去10年入住作者所在医院且诊断为AS的所有患者(22例)。

干预措施

这主要是对眼部特征的回顾,但也记录并讨论了其他特征。

主要观察指标

记录的特征包括视觉症状出现的年龄、畏光情况、视力和视网膜电图检查结果。记录的非眼部特征包括心脏状况、体重和身高、听力以及糖尿病的存在情况。

结果

婴儿期出现的心肌病直到最近才被确认为AS的一个特征。在作者的病例中,22例中有18例患有婴儿期心肌病。在作者所在的三级转诊机构中,存在对年轻患者尤其是非眼部病变患者的确诊偏倚。此外,如果没有婴儿期心肌病的发生,AS在儿童期很难被识别。阿尔斯特伦综合征通常直到第二或第三个十年出现糖尿病时才被识别。最初,可能会诊断为视锥视杆营养不良、全色盲、莱伯先天性黑蒙或巴德-比德尔综合征。在AS中,存在严重的婴儿期视网膜营养不良。视网膜电图缺失或减弱,视杆功能比视锥功能保存得更好。视网膜营养不良呈进行性发展,患者在10岁时视力降至6/60或更低,20岁时无光感。

结论

对于婴儿期视锥和视杆视网膜营养不良,应考虑诊断为AS,特别是如果体重高于第90百分位数(18例中有16例)或存在婴儿期心肌病(22例中有18例)。

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