نتایج جستجو برای: malformation

تعداد نتایج: 15277  

Journal: :Pediatric Neurology Briefs 1990

Journal: :Journal of Pediatric Surgery Case Reports 2018

2007
COLIN L. BERRY JEAN KEELING

Berry, Colin L., Keeling, Jean, and Hilton, Clare (1970). Archives of Disease in Childhood, 45, 229. Coincidence of congenital malformation and embryonic tumours of childhood. Examination of the records of cases of neuroblastoma, nephroblastoma, hepatoblastoma, and teratoma has not revealed a significant association between neoplasia and malformation. An increase in 'local' abnormalities in sac...

Journal: :Turkish neurosurgery 2009
Berker Cemil Kagan Tun Omer Polat Ozlem Ozen Erkan Kaptanoglu

Glioblastoma multiforme is the most common intracranial neoplasm of all primary central nervous system tumors. Glial tumors can present in different forms. Intracranial hemorrhage may occur in all central nervous system tumors to a varying degree and extent and may even be massive. A 58-year-old man presented with intraparenchymal hemorrhage manifesting as severe headache and vomiting. Cranial ...

2005
JULIEN BOGOUSSLAVSKY

A 46-year-old woman under investigation for three episodes of amaurosis fugax in the left eye proved to have a left anterior-middle fossa dural arteriovenous malformation with pial venous drainage. The malformation received its main supply from the left middle meningeal artery, but its anterior part was fed by the recurrent meningeal branch of the left ophthalmic artery. Transient episodic lowe...

Journal: :Journal of medical genetics 2000
S A Lynch Y Wang T Strachan J Burn S Lindsay

Autosomal dominant sacral agenesis is characterised by a partial agenesis of the sacrum typically involving sacral vertebrae S2-S5 only. Associated features include anorectal malformation, a presacral mass, and urogenital malformation. Together, these features have been defined as the Currarino syndrome. Recently, HLXB9 has been identified as the major causative gene in Currarino syndrome allow...

Journal: :Stroke 1985
J Bogousslavsky F Vinuela H J Barnett C G Drake

A 46-year-old woman under investigation for three episodes of amaurosis fugax in the left eye proved to have a left anterior-middle fossa dural arteriovenous malformation with pial venous drainage. The malformation received its main supply from the left middle meningeal artery, but its anterior part was fed by the recurrent meningeal branch of the left ophthalmic artery. Transient episodic lowe...

2014
Huan Wang Bonnie H Wang Kieran P Normoyle Arash Farahvar

While Chiari I malformation is a relatively common finding on MRI imaging, the vast majority of patients are asymptomatic and those who do present typically follow a slow course of chronic or subacute progression of symptoms. Emergent deterioration of existing Chiari malformation is rare. We present two patients with previously undiagnosed Chiari I malformation presenting with acute deteriorati...

Journal: :Neurologia medico-chirurgica 1996
K Shimizu F Yamada S Fukuda S Toya

A 63-year-old male presented with a cerebral arteriovenous malformation in the dominant motor area which subsequently disappeared spontaneously. He had suffered from epileptic attacks in his right extremities for 2 years before he first presented aged 53 years. He was treated with anticonvulsants and was followed up. Bleeding from the cerebral arteriovenous malformation occurred when he was 61 ...

Journal: :Surgical neurology 1984
S S Gebarski H S Greenberg

Cerebral computed tomography (CT) is the primary imaging modality in the investigation of suspected cerebellar degeneration. A case is presented in which an inaccurate clinical and radiologic diagnosis of olivo-pontocerebellar degeneration resulted from CT imaging demonstrating loss of cerebellar substance. Subsequent clinical recognition of downbeat nystagmus led to a diagnosis of Chiari malfo...

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