Skip to main content Accessibility help
×
Hostname: page-component-8448b6f56d-gtxcr Total loading time: 0 Render date: 2024-04-20T02:30:56.328Z Has data issue: false hasContentIssue false

25 - Transplantation of neural stem cells: cellular and gene therapy in pediatric hypoxic–ischemic brain injury

from Part VIII - Neurogenesis and plasticity

Published online by Cambridge University Press:  02 November 2009

Kook In Park
Affiliation:
Department of Pediatrics and Pharmacology, Yonsei University College of Medicine, Seoul, Korea and Departments of Pediatrics, Neurosurgery, & Neurology, Children's Hospital, Boston, MA
Philip E. Stieg
Affiliation:
Department of Neurosurgery, Brigham & Women's Hospital, Harvard Medical School, Boston, MA
Evan Y. Snyder
Affiliation:
Department of Pediatrics, Neurosurgery, & Neurology, Children's Hospital, Boston, MA
Pak H. Chan
Affiliation:
Stanford University, California
Get access

Summary

Introduction

Stroke is the third most common cause of death, and being among the most common causes of severe disability in adults of developed countries accounts for a large proportion of health care costs. Its impact on individual patients, their families and society as a whole is immense. Approximately 200 per 100000 adults per year will have their first stroke. Because the incidence of stroke increases with age, the absolute number of patients with stroke is likely to increase even more, given that the population of aged adults is also increasing. However, brain injury from ischemia does not affect only the adult population. It is a major cause of mortality and severe neurodevelopmental disability (cerebral palsy, mental retardation, epilepsy and learning disabilities) in the pediatric – especially the newborn – population. The drain on resources to support such children (often long into adulthood or an entire lifetime) is also quite significant. Although the etiologies for ischemic brain injury in adults and children may differ, much of the pathophysiology underlying neural cell death and dysfunction is quite similar. In the case of newborn infants, despite advances in technology allowing better obstetric and neonatal care and a deeper understanding of the pathophysiology of perinatal asphyxia, the incidence of hypoxic–ischemic encephalopathy (HIE) in neonates has remained essentially unchanged over the last few decades.

Type
Chapter
Information
Cerebrovascular Disease
22nd Princeton Conference
, pp. 299 - 316
Publisher: Cambridge University Press
Print publication year: 2002

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×