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Published on: June 15, 2011
Unusual clinical presentations in subjects carrying novel NOTCH3 gene mutations
Gabriella Spinicci1, Maria Conti, Maria Valeria Cherchi
1Centro Sclerosi Multipla, Dipartimento di Salute Publica, Medicina Clinica e Molecolare, Università di Cagliari, Caligari, Italy.
Background:
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a disease caused by alterations in the NOTCH3 gene.
Methods:
We describe the clinical, instrumental, and genetic findings in CADASIL patients who carry novel NOTCH3 gene mutations.
Results And Conclusions:
This study broadens the spectrum of clinical manifestations and genetic alterations associated with this disease.
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