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Journal ArticleDOI

Hemimegalencephaly: part 1. Genetic, clinical, and imaging aspects.

Laura Flores-Sarnat
- 01 May 2002 - 
- Vol. 17, Iss: 5, pp 373-384
TLDR
Hemimegalencephaly is a rare hamartomatous malformation of the brain, remarkable for its extreme asymmetry, which can be isolated or associated with several neurocutaneous syndromes; less frequently, it also involves the brain stem and cerebellum.
Abstract
Hemimegalencephaly is a rare hamartomatous malformation of the brain, remarkable for its extreme asymmetry. It can be isolated or associated with several neurocutaneous syndromes; less frequently, it also involves the brain stem and cerebellum. Traditionally, hemimegalencephaly has been considered a primary neuroblast migratory disturbance. At present, genetic theories of pathogenesis and modern histopathology provide a basis for this complex malformation as a primary disturbance in cellular lineage, differentiation, and proliferation, interacting with a disturbance in gene expression of body symmetry, with earlier onset than radial neuroblast migration. From my personal experience with 10 patients with hemimegalencephaly and review of the literature, I have found the same clinical neurologic, neuroimaging, and neuropathologic features in isolated and syndromic hemimegalencephaly. Magnetic resonance imaging (MRI) reveals abnormal gyration, ventriculomegaly, colpocephaly, an "occipital sign" (displacement of the occipital lobe across the midline), and increased volume and T2 signal of white matter, in addition to the overall increased size of the involved hemisphere. Mild, moderate, and severe grades of severity can be recognized, providing a functional neurologic prognosis and therapeutic plan. Early diagnosis is crucial because despite neuroimaging and pathologic evidence, hemimegalencephaly sometimes still is unrecognized. Also, misdiagnosis of obstructive hydrocephalus or cerebral neoplasm can lead to unnecessary surgical procedures. Although hemispherectomy has a high morbidity, it is recommended early for patients with severe, intractable epilepsy. The mildest forms of hemimegalencephaly are infrequent and the least recognized.

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Citations
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Journal ArticleDOI

A Developmental and Genetic Classification for Malformations of Cortical Development: Update 2012.

TL;DR: This review addresses recent changes in the perception of malformations of cerebral cortical development and proposes a modified classification based upon updates in the knowledge of cerebral cortex development.
Journal ArticleDOI

PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasia

TL;DR: This study performs multiplex targeted sequencing of 10 genes in the PI3K/AKT pathway on brain tissue from 33 children who underwent surgical resection of dysplastic cortex for the treatment of intractable epilepsy, finding mutations in PIK3CA and AKT3 are identified as an important cause of epileptogenic brain malformations and establish megalencephaly, hemimegalencephy, and focal cortical dysplasia as part of a single pathogenic spectrum.
Journal ArticleDOI

A developmental and genetic classification for midbrain-hindbrain malformations

TL;DR: A new classification system is proposed, based wherever possible, upon embryology and genetics, for developmental disorders affecting the midbrain and hindbrain that will prove useful for both physicians who diagnose and treat patients with these disorders and for clinical scientists who wish to understand better the perturbations of developmental processes that produce them.
Journal ArticleDOI

Malformations of cortical development and epilepsy.

TL;DR: In this review, the most common malformations or cortical development associated with epilepsy are discussed in regard to their clinical manifestations, classification, imaging appearance and basic neurobiology.
Journal ArticleDOI

Malformations of cortical development and epilepsy.

TL;DR: Malformations of cortical development (MCDs) are macroscopic or microscopic abnormalities of the cerebral cortex that arise as a consequence of an interruption to the normal steps of formation of the cortical plate as mentioned in this paper.
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Journal ArticleDOI

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TL;DR: 5 children described below had an illness characterized by excessively rapid growth, acromegalic features and a nonprogressive cerebral disorder with mental retardation.
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