نتایج جستجو برای: complex vertebral malformation

تعداد نتایج: 824614  

2015
Min Kyung Yu Mo Kyung Jung Ki Eun Kim Ah Reum Kwon Hyun Wook Chae Duk Hee Kim Ho-Seong Kim

Turner syndrome (TS) is a relatively common chromosomal disorder and is associated with a range of comorbidities involving the cardiovascular system. Vascular abnormalities, in particular, are a common finding in cases of TS. However, dissection involving the vertebral arteries is rare. Here, we report the case of a 9-year-old girl with TS who had been treated with growth hormone replacement th...

Journal: :The Thoracic and Cardiovascular Surgeon 2018

Journal: :Ultraschall in der Medizin - European Journal of Ultrasound 2020

Journal: :AJNR. American journal of neuroradiology 2015
M Amarouche J L Hart A Siddiqui T Hampton D C Walsh

BACKGROUND AND PURPOSE The diagnosis of spinal vascular malformations may be challenging on conventional MR imaging because neither the location of the signal abnormality in the spinal cord nor the level of the abnormal flow voids correlates with the level of the fistula. We conducted a retrospective evaluation of the utility of using a time-resolved imaging of contrast kinetics sequence in the...

Journal: :Neurology 2017
Rachid Madkouri Michael Grelat

A 58-year-old man presented to our hospital with cerebellar ataxia, pyramidal signs, dysarthria, bilateral deafness, and cognitive impairment. These symptoms were consistent with superficial siderosis (SS) of the CNS, confirmed by MRI (figure A). Cerebral angiography showed a dural arteriovenous fistula perispinal and pontic with venous drainage in the left foramen C1-C2, fed by meningeal branc...

2013
Allison Tam Kit Shan Lee Sansan Lee William Burkhalter Lucio U. Pascua Thomas P. Slavin

We describe an 8-year-old boy with developmental delay, clinical bilateral radial ulnar synostosis, Klippel-Feil anomaly, and other vertebral deformities who was found to have a de novo deletion of 114.5kb at 16p13.3. The deletion contains five genes and three miRNAs. The genes are E4F1, DNASE1L2, ECI1, RNPS1, and ABCA3; miRNAs are MIR3677, MIR940, and MIR4717. The specific deletion has never b...

Journal: :Postgraduate medical journal 1982
C R Barraclough

The incidence of radiologically demonstrable aneurysm and arteriovenous malformation (AVM) in patients admitted to the Midland Centre for Neurosurgery and Neurology (MCNN) with the diagnosis of spontaneous subarachnoid haemorrhage (SAH) between 1959-80 inclusive was determined. Bilateral carotid angiography (BCA) showed 658% to have one or more aneurysms and 75% an AVM, each figure including 0 ...

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