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Hemihydranencephaly: living with half brain dysfunction
Hemi-hydranencephaly is a very rare condition characterized by complete or almost near-complete unilateral absence of the cortical cortex, which is filled by a sac of cerebrospinal fluid. Prenatal vascular disruption with occlusion of the carotid artery territories ipsilateral to the damaged brain i...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3564735/ https://www.ncbi.nlm.nih.gov/pubmed/23324549 http://dx.doi.org/10.1186/1824-7288-39-3 |
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author | Pavone, Piero Nigro, Francesco Falsaperla, Raffaele Greco, Filippo Ruggieri, Martino Rizzo, Renata Praticò, Andrea D Pavone, Lorenzo |
author_facet | Pavone, Piero Nigro, Francesco Falsaperla, Raffaele Greco, Filippo Ruggieri, Martino Rizzo, Renata Praticò, Andrea D Pavone, Lorenzo |
author_sort | Pavone, Piero |
collection | PubMed |
description | Hemi-hydranencephaly is a very rare condition characterized by complete or almost near-complete unilateral absence of the cortical cortex, which is filled by a sac of cerebrospinal fluid. Prenatal vascular disruption with occlusion of the carotid artery territories ipsilateral to the damaged brain is the presumed pathogenesis. We have selected nine cases that fit the clinical and pathologic characteristics of hemi-hydranencephaly, demonstrating that destruction of one hemisphere may be not always associated with severe neurologic impairment and may allow an almost normal life. This disorder is an example of a possible prenatal re-organization in which the right and left cerebral hemispheres present functional potentiality to make up the damaged brain. The cases reported in the literature are discussed, including a patient previously reported and followed-up for 10 years. A review of the cases is performed with an evaluation of the most important aspect of this rare and mysterious disorder. |
format | Online Article Text |
id | pubmed-3564735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35647352013-02-08 Hemihydranencephaly: living with half brain dysfunction Pavone, Piero Nigro, Francesco Falsaperla, Raffaele Greco, Filippo Ruggieri, Martino Rizzo, Renata Praticò, Andrea D Pavone, Lorenzo Ital J Pediatr Review Hemi-hydranencephaly is a very rare condition characterized by complete or almost near-complete unilateral absence of the cortical cortex, which is filled by a sac of cerebrospinal fluid. Prenatal vascular disruption with occlusion of the carotid artery territories ipsilateral to the damaged brain is the presumed pathogenesis. We have selected nine cases that fit the clinical and pathologic characteristics of hemi-hydranencephaly, demonstrating that destruction of one hemisphere may be not always associated with severe neurologic impairment and may allow an almost normal life. This disorder is an example of a possible prenatal re-organization in which the right and left cerebral hemispheres present functional potentiality to make up the damaged brain. The cases reported in the literature are discussed, including a patient previously reported and followed-up for 10 years. A review of the cases is performed with an evaluation of the most important aspect of this rare and mysterious disorder. BioMed Central 2013-01-16 /pmc/articles/PMC3564735/ /pubmed/23324549 http://dx.doi.org/10.1186/1824-7288-39-3 Text en Copyright ©2013 Pavone et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Pavone, Piero Nigro, Francesco Falsaperla, Raffaele Greco, Filippo Ruggieri, Martino Rizzo, Renata Praticò, Andrea D Pavone, Lorenzo Hemihydranencephaly: living with half brain dysfunction |
title | Hemihydranencephaly: living with half brain dysfunction |
title_full | Hemihydranencephaly: living with half brain dysfunction |
title_fullStr | Hemihydranencephaly: living with half brain dysfunction |
title_full_unstemmed | Hemihydranencephaly: living with half brain dysfunction |
title_short | Hemihydranencephaly: living with half brain dysfunction |
title_sort | hemihydranencephaly: living with half brain dysfunction |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3564735/ https://www.ncbi.nlm.nih.gov/pubmed/23324549 http://dx.doi.org/10.1186/1824-7288-39-3 |
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