Disease #00024 (CADASIL (Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy))

Official abbreviation CADASIL
Name Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
OMIM ID -
Inheritance -
Individuals reported having this disease 6
Phenotype entries for this disease 5
Associated with 1 gene NOTCH3
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Disease features -
Remarks -


Individuals

6 entries on 1 page. Showing entries 1 - 6.
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00000155 Tsun-Haw Toh et al. (2019) M Malaysia Chinese - - - CADASIL - NOTCH3 NOTCH3 1 1 Nuur Athirah Binti Mohd Daud
00000156 Tsun Haw Toh et al. (2019) F Malaysia Chinese - - - CADASIL - NOTCH3 NOTCH3 1 1 Nuur Athirah Binti Mohd Daud
00000157 Tsun Haw Toh et al. (2019) F Malaysia Chinese/Indian - - - CADASIL - NOTCH3 NOTCH3 1 1 Nuur Athirah Binti Mohd Daud
00000158 Tsun Haw Toh et al. (2019) M Malaysia Indian - - - CADASIL - NOTCH3 NOTCH3 1 1 Nuur Athirah Binti Mohd Daud
00000159 Kheng-Seang Lim et al. (2015) - Malaysia Kadazandusun Rungus - - CADASIL - NOTCH3 NOTCH3 2 1 Nuur Athirah Binti Mohd Daud
00000784 Hong Chuan Loh et al.(2021) F Malaysia Chinese-Indian - - - CADASIL First MRI brain scan showed white matter hyperintensities in the periventricular and anterior temporal regions. Second MRI brain scan revealed additional hyperintensity over the left occipital lobe on diffusion-weighted imaging, suggesting a transient ischaemic attack NOTCH3 NOTCH3 1 1 Nur Aisyah Athirah
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