Bridging health care gaps for new survivors – a total population study of young persons with MMC

doi:10.1186/1743-8454-2-S1-S10

Cerebrospinal Fluid Research

Volume 2
Suppl 1

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Mattsson S
Astrom E
Dahl M
Ericsson B
Olsson I
Wendelius M
Westb L

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Astrom E
Dahl M
Ericsson B
Olsson I
Wendelius M
Westb L
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This article is part of the supplement: 49th Annual Meeting of the Society for Research into Hydrocephalus and Spina Bifida .

Oral presentation

Bridging health care gaps for new survivors – a total population study of young persons with MMC

Sven Mattsson , Eva Astrom, Margareta Dahl, Bo Ericsson, Ingrid Olsson, Maggie Wendelius and Lena Westb

Dept of Pediatrics, University Hospital, SE 581 85 Linköping, Sweden

author email corresponding author email

from 49th Annual Meeting of the Society for Research into Hydrocephalus and Spina Bifida
Barcelona, Spain. 29 June – 2 July 2005

Cerebrospinal Fluid Research 2005, 2(Suppl 1):S10doi:10.1186/1743-8454-2-S1-S10


Published:	30 December 2005

First paragraph (this article has no abstract)

Since the number of newborns with myelomeningocele (MMC) is decreasing a national network of neuropaediatricians with long experience of MMC has been founded in Sweden. Our first task was to identify the areas of medical concern in adolescents with MMC.