Results 91 to 100 of about 2,367 (191)

Longitudinal CT and MR appearances of hemimegalencephaly in a patient with tuberous sclerosis

open access: yes, 2008
Case report A 3-day-old baby was referred to our institution with seizures since birth and a presumptive diagnosis of cerebral tumor detected by prenatal ultrasound. Computed tomography (CT) and Magnetic Resonance (MR) imaging performed immediately after
Kesavadas, C   +4 more
core   +1 more source

Pathological differential diagnosis of focal cortical dysplasia type Ⅱ and its mimic lesions

open access: yesChinese Journal of Contemporary Neurology and Neurosurgery, 2020
Malformation of cortical development (MCD) accounts for the majority of drug⁃resistant epilepsy, focal cortica ldysplasia type Ⅱ (FCDⅡ) is the most common and most characteristic. It is of great significance to correct diagnosis for FCDⅡ.
Hai-nan LI, Zhi LI
doaj  

Tuberous Sclerosis Associated with Hemimegalencephaly: A Case Report and Review of the Literature

open access: yes, 2008
  A case of a female infant with tuberous sclerosis and hemimegalencephaly is reported. This full term female infant had tachyarrhythmia on the day of birth, and developed congestive heart failure several days later.
陳慧玲;王本榮;楊千立;廖漢文;沈友仁   +1 more
core  

MRI and 18F-fluorodeoxyglucose positron emission tomography in hemimegalencephaly.

open access: yes, 2000
We report hemimegalencephaly in a 44-year-old woman with mental retardation, epilepsy and a mild hemiparesis. In addition to typical findings on MRI, 2-deoxy-2[18F]fluorodeoxyglucose positron-emission tomography (PET) demonstrated glucose hypometabolism ...
Hoffmann, KT;Amthauer, H;Liebig, T;Hosten, N;Etou, A;Lehmann, TN;Farahati, J;Felix, R
core  

Klippel-Trenaunay-Weber syndrome with hemimegalencephaly. Report of a case

open access: yesThe Turkish Journal of Pediatrics, 1996
A case of Klippel-Trenaunay-Weber Syndrome (KTWS) in a 2.5-year-old girl with congenital hemihypertrophy, nevus flammeus and liver hemangioma is presented. In addition, this report describes the rare association of hemimegalencephaly with KTWS.
F Alpay   +3 more
doaj  

Hemimegalencephaly: 2D, 3D Ultrasound and MRI Correlation

open access: yes, 2010
<i>Background:</i> Hemimegalencephaly (HMC) is a disorder associated with enlarged and dysplastic hamartomatous overgrowth of all or part of the one cerebral hemisphere that can be isolated or associated with other syndromes.
X.C. Romero   +3 more
core   +1 more source

Hemimegalencephalic variant of epidermal nevus syndrome: Case report and literature review.

open access: yes, 2012
The epidermal nevus syndrome (ENS) is an uncommon neurocutaneous disorder in which epidermal nevi are found in association with congenital abnormalities of the brain, eye, and/or skeleton.
CANTALUPO, Gaetano   +12 more
core   +1 more source

A Very Rare Case of Colpocephaly Associated With Trisomy 18

open access: yesGynecology Obstetrics & Reproductive Medicine, 2012
We presented a very rare case of colphocephaly which is a term used to describe a congenital abnormal enlargement of the occipital horns of the lateral ventricules associated with normal frontal horns.
Seyfettin Uludağ   +3 more
doaj  

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