cerebrovascular anomalies

PURPOSE To report prevalence, ocular characteristics and coexisting neurological, behavioural, somatic and neuroradiological… Expand

Noonan syndrome is a common autosomal dominant neurodevelopmental disorder caused by gain-of-function germline mutations… Expand

We report the association of congenital mydriasis with prune belly syndrome and cerebrovascular anomalies in a 9-year-old boy who… Expand

Background:The Bosley-Salih-Alorainy syndrome (BSAS) variant of the congenital human HOXA1 syndrome results from autosomal… Expand

OBJECTIVE To explore the role of and report on congenital and genetic cerebrovascular anomalies as risk factors for stroke in a… Expand

Facial hemangioma is usually isolated but its association with craniocervical arterial anomalies and structural brain… Expand

OBJECTIVE The goal of this study was to describe the expression of matrix proteins and angiogenic factors in cerebrovascular… Expand

Moyamoya syndrome is characterized by the reticulated collateralization of the intracranial vasculature distal to an occlusion of… Expand

A 5-year-old female patient with a left facial strawberry nevus, ipsilateral optic atrophy and cerebellar signs was observed… Expand

It is well known that congenital anomalies such as polycystic kidney, aortic coarctation, Marfan syndrome, Ehler-Danlos syndrome… Expand