A Novel Mutation (C67Y) in the NOTCH3 Gene in a Korean CADASIL Patient.
10.3346/jkms.2003.18.1.141
- Author:
Duk L NA
1
;
So Young MOON
;
Hahn Young KIM
;
Jung Im SEOK
;
Jae Chul KWON
;
Chang Seok KI
;
Jong Won KIM
;
Yeon Lim SUH
Author Information
1. Department of Neurology, Samsung Medical Center, Sungkyunkwan University, School of Medicine, Seoul, Korea. dukna@smc.samsung.co.kr
- Publication Type:Case Report
- Keywords:
CADASIL;
Dementia, Multi-infarct;
Tomography;
Emission-Computed;
The NOTCH3 Gene;
Polymorphism (Genetics)
- MeSH:
Amino Acid Substitution;
Biopsy;
Brain/pathology;
Codon/genetics;
Dementia, Multi-Infarct/diagnosis;
Dementia, Multi-Infarct/genetics*;
Dementia, Multi-Infarct/pathology;
Dementia, Multi-Infarct/radionuclide imaging;
Female;
Human;
Korea;
Magnetic Resonance Imaging;
Middle Aged;
Mutation, Missense*;
Neuropsychological Tests;
Point Mutation*;
Proto-Oncogene Proteins/genetics*;
Skin/pathology;
Tomography, Emission-Computed
- From:Journal of Korean Medical Science
2003;18(1):141-144
- CountryRepublic of Korea
- Language:English
-
Abstract:
We report a 52-yr-old Korean woman with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) whose diagnosis was confirmed by skin biopsy and the presence of a novel mutation in the NOTCH3 gene. The patient's clinical features were rather unusual in that 1) clinical presentations were only two episodes of stroke and mild dementia unaccompanied by mood disturbances or migraine, and 2) there was no family history. Brain MRI showed T2 hyperintensities in both temporal pole areas in line with the recent suggestion by O'Sullivan et al. that the abnormality could be a radiologic marker of CADASIL. FDG-PET also showed a hypometabolism in the temporal pole areas with an abnormal finding on MRI in addition to the hypometabolism in cortical and subcortical regions. We could learn from this case that CADASIL may be included in the differential diagnoses in patients with vascular dementia associated with a small vessel disease, even in the absence of a family history, especially when there are no known stroke risk factors and when the MRI shows T2 hyperintensity in the temporal pole regions.
