Document Detail


Histopathological basis of Horner's syndrome in obstetric brachial plexus palsy differs from that in adult brachial plexus injury.
MedLine Citation:
PMID:  18236458     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Although Horner's syndrome is usually taken as an absolute indicator of avulsions of the C8 and T1 ventral roots in adult brachial plexus injury, its pathological basis in obstetric brachial plexus palsy (OBPP) is unclear. We therefore examined the morphological mechanism for the presence of Horner's syndrome in brachial plexus injury in infants and adults. Some axons of sympathetic preganglionic neurons in T1 innervate the superior cervical ganglion via the C7 ventral root in infants but not in adults. Therefore, the presence of Horner's syndrome may relate in part to avulsion of the C7 root in OBPP. These findings suggest that Horner's syndrome in OBPP is not necessarily indicative of avulsions of the C8 and T1 roots, as it can occur with avulsion of the C7 root.
Authors:
Yi-Gang Huang; Liang Chen; Yu-Dong Gu; Guang-Rong Yu
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Publication Detail:
Type:  Comparative Study; Journal Article    
Journal Detail:
Title:  Muscle & nerve     Volume:  37     ISSN:  0148-639X     ISO Abbreviation:  Muscle Nerve     Publication Date:  2008 May 
Date Detail:
Created Date:  2008-04-16     Completed Date:  2008-06-20     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  7803146     Medline TA:  Muscle Nerve     Country:  United States    
Other Details:
Languages:  eng     Pagination:  632-7     Citation Subset:  IM    
Affiliation:
Department of Orthopaedics, Tong Ji Hospital, Tong Ji University, Shanghai, China.
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MeSH Terms
Descriptor/Qualifier:
Adult
Age Factors
Brachial Plexus Neuropathies / metabolism,  pathology*
Female
Horner Syndrome / etiology*,  metabolism,  pathology*
Humans
Infant
Infant, Newborn
Male
Middle Aged
Nitric Oxide Synthase Type I / metabolism
Paralysis, Obstetric / complications*
Spinal Nerve Roots / metabolism,  pathology
Chemical
Reg. No./Substance:
EC 1.14.13.39/Nitric Oxide Synthase Type I

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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