| Autosomal dominant congenital Horner's syndrome in a Dutch family. | |
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MedLine Citation:
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PMID: 1548493 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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A Dutch family is reported with congenital Horner's syndrome in five cases spanning five generations, with symptoms of varying degree but mainly ptosis and meiosis. Heterochromia iridium, anhidrosis, and enophthalmos were not present. The site of the lesion may be in the region between Gasser's ganglion and the short vertical segment of the internal carotid artery near the siphon. There are only four previous reports showing autosomal dominant inheritance of congenital Horner's syndrome. |
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Authors:
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G Hageman; P F Ippel; F C te Nijenhuis |
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Publication Detail:
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Type: Case Reports; Journal Article |
Journal Detail:
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Title: Journal of neurology, neurosurgery, and psychiatry Volume: 55 ISSN: 0022-3050 ISO Abbreviation: J. Neurol. Neurosurg. Psychiatr. Publication Date: 1992 Jan |
Date Detail:
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Created Date: 1992-04-21 Completed Date: 1992-04-21 Revised Date: 2010-09-07 |
Medline Journal Info:
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Nlm Unique ID: 2985191R Medline TA: J Neurol Neurosurg Psychiatry Country: ENGLAND |
Other Details:
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Languages: eng Pagination: 28-30 Citation Subset: IM |
Affiliation:
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Department of Neurology, Medical Spectrum Twente, Enschede, The Netherlands. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Blepharoptosis
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diagnosis,
genetics Chromosome Aberrations / genetics* Chromosome Disorders Genes, Dominant / genetics* Horner Syndrome / diagnosis, genetics* Humans Male Meiosis / genetics Middle Aged Pedigree |
| Comments/Corrections | |
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