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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Format: | Article |
Language: | English |
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Wiley
2014-01-01
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Series: | Case Reports in Pediatrics |
Online Access: | http://dx.doi.org/10.1155/2014/845074 |
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author | Dilek Sarici Mustafa Ali Akin Selim Kurtoglu Filiz Tubas Serdar Umit Sarici |
author_facet | Dilek Sarici Mustafa Ali Akin Selim Kurtoglu Filiz Tubas Serdar Umit Sarici |
author_sort | Dilek Sarici |
collection | DOAJ |
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). |
format | Article |
id | doaj-art-f04e2c9395784eaa9dfed8d773633649 |
institution | Kabale University |
issn | 2090-6803 2090-6811 |
language | English |
publishDate | 2014-01-01 |
publisher | Wiley |
record_format | Article |
series | Case Reports in Pediatrics |
spelling | doaj-art-f04e2c9395784eaa9dfed8d7736336492025-02-03T01:12:09ZengWileyCase Reports in Pediatrics2090-68032090-68112014-01-01201410.1155/2014/845074845074A Neonate with CLOVES SyndromeDilek Sarici0Mustafa Ali Akin1Selim Kurtoglu2Filiz Tubas3Serdar Umit Sarici4Division of Neonatology, Department of Pediatrics, Erciyes University Faculty of Medicine, 38039 Kayseri, TurkeyDivision of Neonatology, Department of Pediatrics, Erciyes University Faculty of Medicine, 38039 Kayseri, TurkeyDivision of Neonatology, Department of Pediatrics, Erciyes University Faculty of Medicine, 38039 Kayseri, TurkeyDepartment of Pediatrics, Erciyes University Faculty of Medicine, 38039 Kayseri, TurkeyDivision of Neonatology, Department of Pediatrics, Ufuk University Faculty of Medicine, 06500 Ankara, TurkeyCongenital 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).http://dx.doi.org/10.1155/2014/845074 |
spellingShingle | Dilek Sarici Mustafa Ali Akin Selim Kurtoglu Filiz Tubas Serdar Umit Sarici A Neonate with CLOVES Syndrome Case Reports in Pediatrics |
title | A Neonate with CLOVES Syndrome |
title_full | A Neonate with CLOVES Syndrome |
title_fullStr | A Neonate with CLOVES Syndrome |
title_full_unstemmed | A Neonate with CLOVES Syndrome |
title_short | A Neonate with CLOVES Syndrome |
title_sort | neonate with cloves syndrome |
url | http://dx.doi.org/10.1155/2014/845074 |
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