The congenital cranial dysinnervation disorders

2.50
Hdl Handle:
http://hdl.handle.net/11287/593921
Title:
The congenital cranial dysinnervation disorders
Authors:
Gutowski, Nicholas J.; Chilton, J. K.
Abstract:
Congenital cranial dysinnervation disorders (CCDD) encompass a number of related conditions and includes Duane syndrome, congenital fibrosis of the external ocular muscles, Mobius syndrome, congenital ptosis and hereditary congenital facial paresis. These are congenital disorders where the primary findings are non-progressive and are caused by developmental abnormalities of cranial nerves/nuclei with primary or secondary dysinnervation. Several CCDD genes have been found, which enhance our understanding of the mechanisms involved in brain stem development and axonal guidance.
Citation:
Arch Dis Child. 2015 Jul;100(7):678-81.
Publisher:
BMJ
Journal:
Archives of disease in childhood
Issue Date:
1-Jul-2015
URI:
http://hdl.handle.net/11287/593921
DOI:
10.1136/archdischild-2014-307035
PubMed ID:
25633065
Additional Links:
http://adc.bmj.com/cgi/pmidlookup?view=long&pmid=25633065
Note:
RD&E staff can access the full-text of this article by clicking on the 'Additional Link' above and logging in with NHS OpenAthens if prompted.
Type:
Journal Article; Review
Language:
eng
ISSN:
1468-2044
Appears in Collections:
2015 RD&E publications; Neurology

Full metadata record

DC FieldValue Language
dc.contributor.authorGutowski, Nicholas J.en
dc.contributor.authorChilton, J. K.en
dc.date.accessioned2016-01-19T12:37:23Zen
dc.date.available2016-01-19T12:37:23Zen
dc.date.issued2015-07-01en
dc.identifier.citationArch Dis Child. 2015 Jul;100(7):678-81.en
dc.identifier.issn1468-2044en
dc.identifier.pmid25633065en
dc.identifier.doi10.1136/archdischild-2014-307035en
dc.identifier.urihttp://hdl.handle.net/11287/593921en
dc.description.abstractCongenital cranial dysinnervation disorders (CCDD) encompass a number of related conditions and includes Duane syndrome, congenital fibrosis of the external ocular muscles, Mobius syndrome, congenital ptosis and hereditary congenital facial paresis. These are congenital disorders where the primary findings are non-progressive and are caused by developmental abnormalities of cranial nerves/nuclei with primary or secondary dysinnervation. Several CCDD genes have been found, which enhance our understanding of the mechanisms involved in brain stem development and axonal guidance.en
dc.language.isoengen
dc.publisherBMJen
dc.relation.urlhttp://adc.bmj.com/cgi/pmidlookup?view=long&pmid=25633065en
dc.titleThe congenital cranial dysinnervation disordersen
dc.typeJournal Articleen
dc.typeReviewen
dc.identifier.journalArchives of disease in childhooden
dc.description.noteRD&E staff can access the full-text of this article by clicking on the 'Additional Link' above and logging in with NHS OpenAthens if prompted.en

Related articles on PubMed

All Items in RD&E Research Repository are protected by copyright, with all rights reserved, unless otherwise indicated.