neuronal heterotopia
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2019 ◽  
Vol 10 ◽  
Author(s):  
Regina Vontell ◽  
Veena G. Supramaniam ◽  
Alice Davidson ◽  
Claire Thornton ◽  
Andreas Marnerides ◽  
...  

2019 ◽  
Vol 25 (4) ◽  
pp. 561-568 ◽  
Author(s):  
Johannes Klaus ◽  
Sabina Kanton ◽  
Christina Kyrousi ◽  
Ane Cristina Ayo-Martin ◽  
Rossella Di Giaimo ◽  
...  
Keyword(s):  

2018 ◽  
Vol 149 (suppl_1) ◽  
pp. S60-S61
Author(s):  
Yasir AlZubaidi ◽  
Jehan Abdulsattar ◽  
Guillermo Herrera ◽  
Firas Al-Delfi

2017 ◽  
Vol 21 ◽  
pp. e189-e190
Author(s):  
Valentina Ivanovna Guzeva ◽  
Inna Vladimirovna Ochrim ◽  
Oksana Valentinovna Guzeva ◽  
Viktoria Valentinovna Guzeva ◽  
Nadezhda Evgenevna Maksimova

2016 ◽  
Vol 59 (2) ◽  
pp. E17-E21 ◽  
Author(s):  
Antonia DeJesus ◽  
Bradley J. Turek ◽  
Evelyn Galban ◽  
Jantra Ngosuwan Suran

2014 ◽  
Vol 17 (7) ◽  
pp. 923-933 ◽  
Author(s):  
Michel Kielar ◽  
Françoise Phan Dinh Tuy ◽  
Sara Bizzotto ◽  
Cécile Lebrand ◽  
Camino de Juan Romero ◽  
...  
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2014 ◽  
Vol 4 ◽  
pp. 22 ◽  
Author(s):  
Harun Arslan ◽  
Metin Saylık ◽  
Hüseyin Akdeniz

Ectopic neurohypophysis is a pituitary gland abnormality, which can accompany growth hormone deficiency associated with dwarfism. Here we present magnetic resonance imaging (MRI) findings of a rare case of ectopic neurohypophysis, corpus callosum dysgenesis, and periventricular neuronal heterotopia coexisting, with a review of the literature.


2006 ◽  
Vol 12 (2) ◽  
pp. 99-105
Author(s):  
Vera C. Terra-Bustamante ◽  
Hélio R. Machado ◽  
Américo C. Sakamoto

INTRODUCTION: Cerebral cortical development is a highly complex process influenced by environmental, genetic and functional abnormalities. Hemimegalencephaly (HME) is a rare brain malformation that involves overgrowth of one hemisphere. Clinically macrocephaly, mental retardation, contralateral hemiparesis, hemianopsia and intractable epilepsy may be present. Diagnosis is mainly done with image and clinical findings. MRI typically reveals an enlarged cerebrum involving at least one lobe, with a thickened cortex; broad gyres; abnormal gray-white matter differentiation with abnormal sign; neuronal heterotopia, ventricle asymmetry, and basal ganglia and internal capsule abnormalities. Electroencephalographic abnormalities usually involve the affected hemisphere, with an asymmetric amplitude of the normal, age-related rhythms; slow, rhythmic or fast activity and multifocal unilateral or bilateral high-amplitude spikes and spike-wave complexes. Histopathologic changes include abnormal gyrification, with loss of cortical lamination, neuronal heterotopia, gliosis, large bizarre neurons and balloon-cells. The presence of highly refractory seizures in patients with HME is an important factor to consider epilepsy surgery in these patients. METHODS: Multiple surgical techniques are actually being used for hemispheric disconnection. We discuss here the main surgical techniques that are used for hemispheric disconnection. CONCLUSIONS: Postsurgery outcome for HME may be not as good as that for focal lesions with approximately 40% of patients being seizure free, but the main indication for surgery in these patients may be preventing additional cognitive injury and developmental delay. Surgical complications are observed in most of the series of patients with HME submitted to hemispheric surgery. Minimal resections may contribute do diminish surgical complications.


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