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A Neonate with CLOVES Syndrome
Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE) syndrome is a recently delineated disorder that comprises vascular malformations (typically truncal), dysregulated adipose tissue, scoliosis, enlarged bony structures (typically of the legs) without progression, or...
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Published in: | Case reports in pediatrics 2014-01, Vol.2014 (2014), p.1-2 |
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description | Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE) syndrome is a recently delineated disorder that comprises vascular malformations (typically truncal), dysregulated adipose tissue, scoliosis, enlarged bony structures (typically of the legs) without progression, or distorting bony overgrowth. The name CLOVE was subsequently extended to CLOVES to emphasize the association with scoliosis/skeletal and spinal anomalies and seizures/central nervous system malformations. We herein report a very rare case of CLOVES syndrome with the findings of lipomatous overgrowth in the cheek (facial asymmetry), vascular malformation (hemangiomas), epidermal nevi (large port wine stains), and skeletal abnormalities (widened first interdigital space, dystrophia in the nail of the first digit of the right foot, and bilateral hypertrophy of the first digits of the feet). |
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The name CLOVE was subsequently extended to CLOVES to emphasize the association with scoliosis/skeletal and spinal anomalies and seizures/central nervous system malformations. We herein report a very rare case of CLOVES syndrome with the findings of lipomatous overgrowth in the cheek (facial asymmetry), vascular malformation (hemangiomas), epidermal nevi (large port wine stains), and skeletal abnormalities (widened first interdigital space, dystrophia in the nail of the first digit of the right foot, and bilateral hypertrophy of the first digits of the feet).</description><identifier>ISSN: 2090-6803</identifier><identifier>EISSN: 2090-6811</identifier><identifier>DOI: 10.1155/2014/845074</identifier><identifier>PMID: 25400966</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Case Report</subject><ispartof>Case reports in pediatrics, 2014-01, Vol.2014 (2014), p.1-2</ispartof><rights>Copyright © 2014 Dilek Sarici et al.</rights><rights>Copyright © 2014 Dilek Sarici et al. Dilek Sarici et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2014 Dilek Sarici et al. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c463t-58fdde17d4421d50778f53eddcd23a21f08159416d79e3fc6dc8863cb0b5f9f13</citedby><cites>FETCH-LOGICAL-c463t-58fdde17d4421d50778f53eddcd23a21f08159416d79e3fc6dc8863cb0b5f9f13</cites><orcidid>0000-0002-7671-3010</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1619273420/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1619273420?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25400966$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Cogulu, Ozgur</contributor><creatorcontrib>Tubas, Filiz</creatorcontrib><creatorcontrib>Kurtoglu, Selim</creatorcontrib><creatorcontrib>Akin, Mustafa Ali</creatorcontrib><creatorcontrib>Sarici, Dilek</creatorcontrib><creatorcontrib>Sarici, Serdar Umit</creatorcontrib><title>A Neonate with CLOVES Syndrome</title><title>Case reports in pediatrics</title><addtitle>Case Rep Pediatr</addtitle><description>Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE) syndrome is a recently delineated disorder that comprises vascular malformations (typically truncal), dysregulated adipose tissue, scoliosis, enlarged bony structures (typically of the legs) without progression, or distorting bony overgrowth. 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The name CLOVE was subsequently extended to CLOVES to emphasize the association with scoliosis/skeletal and spinal anomalies and seizures/central nervous system malformations. We herein report a very rare case of CLOVES syndrome with the findings of lipomatous overgrowth in the cheek (facial asymmetry), vascular malformation (hemangiomas), epidermal nevi (large port wine stains), and skeletal abnormalities (widened first interdigital space, dystrophia in the nail of the first digit of the right foot, and bilateral hypertrophy of the first digits of the feet).</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>25400966</pmid><doi>10.1155/2014/845074</doi><tpages>2</tpages><orcidid>https://orcid.org/0000-0002-7671-3010</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Case Report |
title | A Neonate with CLOVES Syndrome |
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