Bilateral Multilevel Cervical Rib and Bilateral Omovertebra in Klippel-Feil Syndrome

BACKGROUNDKlippel-Feil syndrome was first described in 1912; a short neck, low posterior hairline, and decreased cervical joint range of motion are the classical triad of this disease. In this syndrome, which is rarely observed, the characteristics that have been reported include the following: scol...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:World neurosurgery 2020, Vol.136, p.62-65
Hauptverfasser: Satış, Serap, Alparslan, Nur, Tuna, Mustafa, Dere, Osman, Yetişgin, Alparslan
Format: Report
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 65
container_issue
container_start_page 62
container_title World neurosurgery
container_volume 136
creator Satış, Serap
Alparslan, Nur
Tuna, Mustafa
Dere, Osman
Yetişgin, Alparslan
description BACKGROUNDKlippel-Feil syndrome was first described in 1912; a short neck, low posterior hairline, and decreased cervical joint range of motion are the classical triad of this disease. In this syndrome, which is rarely observed, the characteristics that have been reported include the following: scoliosis; Sprengel deformity; cervical rib; ear, nose, oral, and laryngeal abnormalities; structural abnormalities of the urinary system; and congenital heart diseases. However, bilateral omovertebra and bilateral multilevel cervical ribs have not been reported. CASE DESCRIPTIONWe aimed to present this rare syndrome via radiologic findings from cases with bilateral multilevel cervical rib and bilateral omovertebra. CONCLUSIONSCases of Klippel-Feil syndrome may be accompanied by multiple abnormalities. We want to highlight the need for detailed examination of patients and lifestyle modification at an early age, before symptom appearance, as well as adaptation to habitual exercise.
doi_str_mv 10.1016/j.wneu.2020.01.010
format Report
fullrecord <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_miscellaneous_2338101300</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2338101300</sourcerecordid><originalsourceid>FETCH-proquest_miscellaneous_23381013003</originalsourceid><addsrcrecordid>eNqVjrEKwjAURYMgKNofcMro0po0YuNqsQgignYvaX1C5DWtSVvx780gOHu5cOFyhkPIgrOIM75ZPaKXgT6KWcwixn3ZiEy5TGQok812QgLnHsxH8LVMxJTkO42qA6uQnnrsNMIASFOwg678d9ElVeZGf9S5bgawHZRWUW3oEXXbAoYZaKTXt7nZpoY5Gd8VOgi-OyPLbJ-nh7C1zbMH1xW1dhUgKgNN74pYCOnthdf6A_0AzAlKcQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>report</recordtype><pqid>2338101300</pqid></control><display><type>report</type><title>Bilateral Multilevel Cervical Rib and Bilateral Omovertebra in Klippel-Feil Syndrome</title><source>Elsevier ScienceDirect Journals Complete</source><creator>Satış, Serap ; Alparslan, Nur ; Tuna, Mustafa ; Dere, Osman ; Yetişgin, Alparslan</creator><creatorcontrib>Satış, Serap ; Alparslan, Nur ; Tuna, Mustafa ; Dere, Osman ; Yetişgin, Alparslan</creatorcontrib><description>BACKGROUNDKlippel-Feil syndrome was first described in 1912; a short neck, low posterior hairline, and decreased cervical joint range of motion are the classical triad of this disease. In this syndrome, which is rarely observed, the characteristics that have been reported include the following: scoliosis; Sprengel deformity; cervical rib; ear, nose, oral, and laryngeal abnormalities; structural abnormalities of the urinary system; and congenital heart diseases. However, bilateral omovertebra and bilateral multilevel cervical ribs have not been reported. CASE DESCRIPTIONWe aimed to present this rare syndrome via radiologic findings from cases with bilateral multilevel cervical rib and bilateral omovertebra. CONCLUSIONSCases of Klippel-Feil syndrome may be accompanied by multiple abnormalities. We want to highlight the need for detailed examination of patients and lifestyle modification at an early age, before symptom appearance, as well as adaptation to habitual exercise.</description><identifier>EISSN: 1878-8769</identifier><identifier>DOI: 10.1016/j.wneu.2020.01.010</identifier><language>eng</language><ispartof>World neurosurgery, 2020, Vol.136, p.62-65</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>776,780,4476,27902</link.rule.ids></links><search><creatorcontrib>Satış, Serap</creatorcontrib><creatorcontrib>Alparslan, Nur</creatorcontrib><creatorcontrib>Tuna, Mustafa</creatorcontrib><creatorcontrib>Dere, Osman</creatorcontrib><creatorcontrib>Yetişgin, Alparslan</creatorcontrib><title>Bilateral Multilevel Cervical Rib and Bilateral Omovertebra in Klippel-Feil Syndrome</title><title>World neurosurgery</title><description>BACKGROUNDKlippel-Feil syndrome was first described in 1912; a short neck, low posterior hairline, and decreased cervical joint range of motion are the classical triad of this disease. In this syndrome, which is rarely observed, the characteristics that have been reported include the following: scoliosis; Sprengel deformity; cervical rib; ear, nose, oral, and laryngeal abnormalities; structural abnormalities of the urinary system; and congenital heart diseases. However, bilateral omovertebra and bilateral multilevel cervical ribs have not been reported. CASE DESCRIPTIONWe aimed to present this rare syndrome via radiologic findings from cases with bilateral multilevel cervical rib and bilateral omovertebra. CONCLUSIONSCases of Klippel-Feil syndrome may be accompanied by multiple abnormalities. We want to highlight the need for detailed examination of patients and lifestyle modification at an early age, before symptom appearance, as well as adaptation to habitual exercise.</description><issn>1878-8769</issn><fulltext>true</fulltext><rsrctype>report</rsrctype><creationdate>2020</creationdate><recordtype>report</recordtype><recordid>eNqVjrEKwjAURYMgKNofcMro0po0YuNqsQgignYvaX1C5DWtSVvx780gOHu5cOFyhkPIgrOIM75ZPaKXgT6KWcwixn3ZiEy5TGQok812QgLnHsxH8LVMxJTkO42qA6uQnnrsNMIASFOwg678d9ElVeZGf9S5bgawHZRWUW3oEXXbAoYZaKTXt7nZpoY5Gd8VOgi-OyPLbJ-nh7C1zbMH1xW1dhUgKgNN74pYCOnthdf6A_0AzAlKcQ</recordid><startdate>20200401</startdate><enddate>20200401</enddate><creator>Satış, Serap</creator><creator>Alparslan, Nur</creator><creator>Tuna, Mustafa</creator><creator>Dere, Osman</creator><creator>Yetişgin, Alparslan</creator><scope>7X8</scope></search><sort><creationdate>20200401</creationdate><title>Bilateral Multilevel Cervical Rib and Bilateral Omovertebra in Klippel-Feil Syndrome</title><author>Satış, Serap ; Alparslan, Nur ; Tuna, Mustafa ; Dere, Osman ; Yetişgin, Alparslan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_23381013003</frbrgroupid><rsrctype>reports</rsrctype><prefilter>reports</prefilter><language>eng</language><creationdate>2020</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Satış, Serap</creatorcontrib><creatorcontrib>Alparslan, Nur</creatorcontrib><creatorcontrib>Tuna, Mustafa</creatorcontrib><creatorcontrib>Dere, Osman</creatorcontrib><creatorcontrib>Yetişgin, Alparslan</creatorcontrib><collection>MEDLINE - Academic</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Satış, Serap</au><au>Alparslan, Nur</au><au>Tuna, Mustafa</au><au>Dere, Osman</au><au>Yetişgin, Alparslan</au><format>book</format><genre>unknown</genre><ristype>RPRT</ristype><atitle>Bilateral Multilevel Cervical Rib and Bilateral Omovertebra in Klippel-Feil Syndrome</atitle><jtitle>World neurosurgery</jtitle><date>2020-04-01</date><risdate>2020</risdate><volume>136</volume><spage>62</spage><epage>65</epage><pages>62-65</pages><eissn>1878-8769</eissn><abstract>BACKGROUNDKlippel-Feil syndrome was first described in 1912; a short neck, low posterior hairline, and decreased cervical joint range of motion are the classical triad of this disease. In this syndrome, which is rarely observed, the characteristics that have been reported include the following: scoliosis; Sprengel deformity; cervical rib; ear, nose, oral, and laryngeal abnormalities; structural abnormalities of the urinary system; and congenital heart diseases. However, bilateral omovertebra and bilateral multilevel cervical ribs have not been reported. CASE DESCRIPTIONWe aimed to present this rare syndrome via radiologic findings from cases with bilateral multilevel cervical rib and bilateral omovertebra. CONCLUSIONSCases of Klippel-Feil syndrome may be accompanied by multiple abnormalities. We want to highlight the need for detailed examination of patients and lifestyle modification at an early age, before symptom appearance, as well as adaptation to habitual exercise.</abstract><doi>10.1016/j.wneu.2020.01.010</doi></addata></record>
fulltext fulltext
identifier EISSN: 1878-8769
ispartof World neurosurgery, 2020, Vol.136, p.62-65
issn 1878-8769
language eng
recordid cdi_proquest_miscellaneous_2338101300
source Elsevier ScienceDirect Journals Complete
title Bilateral Multilevel Cervical Rib and Bilateral Omovertebra in Klippel-Feil Syndrome
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-18T23%3A07%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:book&rft.genre=unknown&rft.atitle=Bilateral%20Multilevel%20Cervical%20Rib%20and%20Bilateral%20Omovertebra%20in%20Klippel-Feil%20Syndrome&rft.jtitle=World%20neurosurgery&rft.au=Sat%C4%B1%C5%9F,%20Serap&rft.date=2020-04-01&rft.volume=136&rft.spage=62&rft.epage=65&rft.pages=62-65&rft.eissn=1878-8769&rft_id=info:doi/10.1016/j.wneu.2020.01.010&rft_dat=%3Cproquest%3E2338101300%3C/proquest%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2338101300&rft_id=info:pmid/&rfr_iscdi=true