Unveiling a Neurological Enigma: Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) Presenting With Facial Palsy

Author:

Jain Sakshi,Sirekulam Vaishnavi,Kinthada SudhaRani,Patel Rashi Bharat,Naik Nishthaben,Jain Shikha,Khan Tanzina,Gill Harmeet,Patel Neel,Nanjundappa Athmananda,Vala Lovekumar,Siripuram Chandu

Publisher

Springer Science and Business Media LLC

Reference14 articles.

1. Genetic spectrum of NOTCH3 and clinical phenotype of CADASIL patients in different populations;Ni W;CNS Neurosci Ther,2022

2. CADASIL: imaging characteristics and clinical correlation;Zhu S;Curr Pain Headache Rep,2016

3. [CADASIL: a case series of 11 patients];Vázquez do Campo R;Rev Neurol,2011

4. A novel NOTCH3 gene mutation in a polish CADASIL family;Machowska-Sempruch K;J Stroke Cerebrovasc Dis,2019

5. [From gene to disease; from Notch3 to cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy];Oberstein SA;Ned Tijdschr Geneeskd,2001

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