一例类卡恩斯-塞尔综合征罕见病例报告。

A report on a rare case of Kearns Sayre-like syndrome.

作者信息

Gupta Y, Gupta M, Sambhav K, Phougat A, Varshney A

机构信息

Medical College, AMU, Aligarh, India.

出版信息

Nepal J Ophthalmol. 2010 Jul-Dec;2(2):160-3. doi: 10.3126/nepjoph.v2i2.3725.

DOI:10.3126/nepjoph.v2i2.3725

PMID:21505535

Abstract

To report the presentation of a rare case of Kearns-Sayre-like syndrome (KSS) CASE: A 14-year-old boy presented with progressive drooping of both upper eyelids for 10 years. Past history of right sided hemi-plegia and left facial nerve palsy was present. Examination (OU) showed total external ophthalmoplegia, ptosis and pigmentary retinopathy. The patient also had a short stature (height 121.9 cm) for his age.

摘要

报告一例罕见的类凯-赛综合征（KSS）病例病例：一名14岁男孩，双侧上睑进行性下垂10年。既往有右侧偏瘫和左侧面神经麻痹病史。检查（双眼）显示完全性眼外肌麻痹、上睑下垂和色素性视网膜病变。该患者按其年龄身高也较矮（身高121.9厘米）。