A Case of Klippel-Feil Syndrome combined with Duane Retraction Syndrome: Incomplete Form of Wildervanck Syndrome.
- Author:
Ki Hwang LEE
1
;
Sang Ho MOON
;
Jun Bum KIM
;
Jae Ho CHO
;
Yoon Hee CHANG
Author Information
1. Department of Ophthalmology, Ajou University School of Medicine, Suwon, Korea. yhchang@ajou.ac.kr.
- Publication Type:Case Report
- Keywords:
Duane retraction syndrome;
Klippel-Feil syndrome;
Wildervanck syndrome
- MeSH:
Adolescent;
Cervical Vertebrae;
Duane Retraction Syndrome*;
Esotropia;
Female;
Hair;
Head;
Hearing Loss;
Humans;
Klippel-Feil Syndrome*;
Neck;
Parturition;
Spine;
Visual Acuity
- From:Journal of the Korean Ophthalmological Society
2005;46(6):1084-1088
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: Klippel-Feil syndrome is defined as the congenital fusion of two or more cervical vertebrae. The clinical features are low posterior hair line, short neck, and limitation of the movement of the head and neck. Wildervanck syndrome, also known as cervicooculoacoustic syndrome, is a rare genetic disorder that primarily affects females. The disorder is characterized by Klippel-Feil syndrome, Duane syndrome and hearing impairment at birth, although one of these symptoms may be lacking. This report describes a case of Klippel-Feil syndrome combined with Duane retraction syndrome, which can be defined as an incomplete form of Wildervanck syndrome. METHODS: A 15-year-old girl with congenitally fused cervical vertebrae at two levels, C2-C4 vertebrae and, C5-C7 vertebrae, was diagnosed as Klippel-Feil syndrome. Ophthalmologic evaluation was needed due to abnormality in ocular motility. RESULTS: Ophthalmologic examination revealed a visual acuity of 0.9 without correction in both eyes. Slit-lamp and fundus examination were normal. Ocular motility examination showed 14 prism diopters right esotropia in primary gaze, limited abduction, globe retraction, and narrowing of the palpebral fissure on adduction of the right eye.
