نتایج جستجو برای: cerebral hypoplasia

تعداد نتایج: 190289  

2015
Zhi-Yong Zhang Shoichiro Sato Lei Liu Shuang Xue Zun-Jing Liu Zhao-Hui Tian Wei Liu Kazunori Toyoda Jin-Song Jiao

To the Editor: A 36‐year‐old man with intermittent migraine‐like headache with aura for 20 years underwent cerebrovascular computed tomography angiography (CTA) revealing very small calibers of bilateral internal carotid arteries (ICAs) in other hospital. He was admitted to our hospital for further examination several days later. He had no vascular risk factors, and no family history of atheros...

Journal: :dental research journal 0
nasim jafari-pozve mahnaz sheikhi masoud ataie-khorasgani shahram jafari-pozve

maxillary sinus aplasia and hypoplasia are rare conditions that can cause symptoms such as headaches and voice alteration. the majority of patients are asymptomatic, but these conditions must be noticed for importance of differential diagnosis such as infection and neoplasms. conventional radiographs could not differentiate between infl ammatory mucosal thickening, neoplasm, and hypoplasia of t...

Journal: :Turkish neurosurgery 2016
Ayse Karatas Hakan Yilmaz Gokmen Coban Murat Koker Aysun Uz

AIM The function of the circle of Willis, an arterial polygon, is to protect the brain from ischemia. The aim of this study is to define the structural characteristics of the circle of Willis within the Turkish adult population, along with variations and arteries involved in the measurement of diameters and lengths on cadavers. MATERIAL AND METHODS The circle of Willis was evaluated in 100 fr...

2011
Yasmin Namavar Peter G Barth Bwee Tien Poll-The Frank Baas

Pontocerebellar Hypoplasia (PCH) is group of very rare, inherited progressive neurodegenerative disorders with prenatal onset. Up to now seven different subtypes have been reported (PCH1-7). The incidence of each subtype is unknown. All subtypes share common characteristics, including hypoplasia/atrophy of cerebellum and pons, progressive microcephaly, and variable cerebral involvement. Patient...

Journal: :AJNR. American journal of neuroradiology 1996
A M Tokumaru A J Barkovich S F Ciricillo M S Edwards

PURPOSE To analyze the skull and brain malformations in patients with craniofacial syndromes. METHODS A retrospective analysis of imaging studies of 21 children with craniofacial anomalies (8 with Apert syndrome, 6 with Pfeiffer syndrome, 4 with Crouzon syndrome, 1 with Robert syndrome, 1 with Coffin-Lowry-syndrome, and 1 with Saethre-Chotzen syndrome) was carried out using CT (21 patients), ...

Journal: :Stroke 1993
S Kazui T Sawada H Naritomi Y Kuriyama T Yamaguchi

BACKGROUND AND PURPOSE Brain infarction localized in the anterior cerebral artery territory is rather uncommon, and its etiology has not yet been fully elucidated. METHODS Based on computed tomographic findings, 17 patients with solitary anterior cerebral artery territory infarction were selected from among 3,619 patients admitted consecutively to our institute. Patients without angiographic ...

2009
Hana Abouzeid Mohamed A. Youssef Nihal ElShakankiri Philippe Hauser Francis L. Munier Daniel F. Schorderet

PURPOSE To report the clinical and genetic study of patients with autosomal dominant aniridia. METHODS We studied ten patients with aniridia from three families of Egyptian origin. All patients underwent full ophthalmologic, general and neurological examination, and blood drawing. Cerebral magnetic resonance imaging was performed in the index case of each family. Genomic DNA was prepared from...

Journal: :Brain : a journal of neurology 2013
Thomas D Cushion William B Dobyns Jonathan G L Mullins Neil Stoodley Seo-Kyung Chung Andrew E Fry Ute Hehr Roxana Gunny Arthur S Aylsworth Prab Prabhakar Gökhan Uyanik Julia Rankin Mark I Rees Daniela T Pilz

Polymicrogyria and lissencephaly are causally heterogeneous disorders of cortical brain development, with distinct neuropathological and neuroimaging patterns. They can be associated with additional structural cerebral anomalies, and recurrent phenotypic patterns have led to identification of recognizable syndromes. The lissencephalies are usually single-gene disorders affecting neuronal migrat...

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