نتایج جستجو برای: hemimegalencephaly

تعداد نتایج: 239  

Journal: :Journal of Pediatric Neurosciences 2015

2006
LUCIANO DE PAOLA 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...

Journal: :iranian journal of child neurology 0
farhad heydarian md, associate professor of pediatrics, mashhad university of medical sciences, mashhad, iran farah ashrafzadeh md, pediatric neurologist,professor of pediatrics, mashhad university of medical sciences,mashhad, iran mahmoud taheri heravi associate professor of radiology, mashhad university of medical sciences,mashhad, iran

objective proteus syndrome is an extremely rare, sporadic and progressive disorder. we describe a four-month-old male baby with central nervous system manifestations in this article. clinical presentation a four-month-old boy was admitted into our hospital with three tonic - clonic generalized seizure attacks which started from the day before admission. each seizure attack lasted less than 10 m...

Journal: :AJNR. American journal of neuroradiology 1998
P D Griffiths S A Gardner M Smith C Rittey T Powell

We describe two children with complex cortical malformations as well as the typical intracranial manifestations of tuberous sclerosis complex. One child had hemimegalencephaly and the other had extensive focal megalencephaly. These cases are discussed in terms of the current concepts of cortical malformations.

Journal: :Seizure 2008
Halisson Bastos Paula Fabiana Sobral da Silva Marco Antônio Veloso de Albuquerque Adriana Mattos Rudimar Santos Riesgo Lygia Ohlweiler Maria Isabel Bragatti Winckler José Augusto Bragatti Rodrigo Dias Duarte Denise Isabel Zandoná

The authors report two cases of Brazilian children with most of the common syndromic features of Proteus syndrome, such as asymmetric overgrowth of tissues, skin abnormalities, hypotonia and mental retardation. In both patients, a refractory epilepsy, compatible with Ohtahara syndrome, as well as hemimegalencephaly, with asymmetric distribution of facial fat, were also diagnosed.

Journal: :AJNR. American journal of neuroradiology 1995
J M Mathis J D Barr A L Albright J A Horton

A patient with hemimegalencephaly and intractable epilepsy underwent a preoperative embolic hemispherectomy. A seizure-free interval of 1 year followed the embolization procedure. In addition, the procedure was thought to be beneficial in limiting blood loss during a subsequent surgical hemispherectomy.

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