Gillespie Syndrome with Partial Aniridia, Cerebellar Ataxia, Delayed Development: A case report.
- Author:
Sung Koo CHANG
1
;
Hyeon Il OH
;
Yeo Jyne YOO
;
Si Hyun AHN
;
Ik Hwan JANG
Author Information
1. Department of Rehabilitation Medicine, Dongrae Bong Seng Hospital.
- Publication Type:Case Report
- Keywords:
Gillespie syndrome;
Partial aniridia;
Cerebellar ataxia;
Mental retardation;
Delayed development
- MeSH:
Aniridia*;
Australia;
Belgium;
Brain;
Brazil;
Cerebellar Ataxia*;
Child, Preschool;
Female;
Humans;
Intellectual Disability;
Ireland;
Korea;
Magnetic Resonance Imaging
- From:Journal of the Korean Academy of Rehabilitation Medicine
1999;23(1):181-185
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
In 1965 Gillespie reported a new syndrome of bilateral aniridia, cerebellar ataxia, and oligophrenia (mental retardation). This new syndrome was named Gillespie syndrome. Since then only 17 cases of Gillespie syndrome have been reported in UK, Brazil, Ireland, Belgium, Australia, and US. A case of Gillespie syndrome was not reported in Korea. A 4 year-old girl has triad of Gillespie syndrome, which are partial aniridia, cerebellar ataxia and mental retardation. We confirmed this with ophthalmologic examination, brain MRI, and developmental delay. We report the typical manifestation of Gillespie syndrome in a 4 year-old girl with the brief review of literature.
