a ayood helo 17 éve
279
Young adult Neurology
CADASIL, a genetic disorder tied to the NOTCH3 gene on chromosome 19, is often characterized by early occurrences of cerebral vascular accidents, dementia, and migraine-like headaches.
a ayood helo 17 éve
279
Még több ilyen
late onset metabolics
Neuro raheumatolgic
CADASIL
CADASIL: WM lesion are lacunes that can mimic MS on MRI; lesions affects tips of anterior
temporals symmetrically. characteristiclly h/o maigraine like headache and h/o early family CVA.
the characteristic lacunes are sub cortical which differentiate it from the deep lacunes from HTN.
presentations: early CVA; early dementia, migraine.
etiology: NOTCH3 gene on chromosme 19
MS
