A Case of Tuberous Sclerosis with Hemimegalencephaly.
- Author:
Yoon Jung LEE
1
;
Eun Hye LEE
;
Min Hee JUNG
;
Mi Sun YUM
;
Tae Sung KO
Author Information
1. Department of Pediatrics, Asan Medical Center, University of Ulsan College of Medicine, Korea. tsko@amc.seoul.kr
- Publication Type:Case Report
- Keywords:
Tuberous sclerosis;
Hemimegalencephaly;
Epilepsy
- MeSH:
Epilepsy;
Malformations of Cortical Development;
Neurocutaneous Syndromes;
Seizures;
Tuberous Sclerosis
- From:
Journal of the Korean Child Neurology Society
2009;17(2):231-236
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Hemimegalencephaly and tuberous sclerosis complex are distinct and rare conditions which are characterized by malformations of cortical developments. Hemimegalencephaly is a cerebral malformation of unknown pathophysiology characterized by asymmetry of the hemispheres and cortical dysplasia. Tuberous sclerosis complex(TSC) is an autosomal dominant neurocutaneous disorder characterized by the formation of hamartomatous lesion in multiple organ systems. While they are currently thought to be unrelated, there are similar cases in the literature and it is conceivable that an abnormality in early cortical development could lead to both conditions in an individual. We report here a first Korean case of unusual association of hemimegalencephaly and tuberous sclerosis complex with mutation in the TSC2 gene, who presented initially frequent partial seizures and infantile spasms.
