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Prenatal diagnosis of Caudal Regression Syndrome : a case report

BACKGROUND: Caudal regression is a rare syndrome which has a spectrum of congenital malformations ranging from simple anal atresia to absence of sacral, lumbar and possibly lower thoracic vertebrae, to the most severe form which is known as sirenomelia. Maternal diabetes, genetic predisposition and...

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Autores principales: Aslan, Halil, Yanik, Halil, Celikaslan, Nurgul, Yildirim, Gokhan, Ceylan, Yavuz
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC64494/
https://www.ncbi.nlm.nih.gov/pubmed/11782287
http://dx.doi.org/10.1186/1471-2393-1-8
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author Aslan, Halil
Yanik, Halil
Celikaslan, Nurgul
Yildirim, Gokhan
Ceylan, Yavuz
author_facet Aslan, Halil
Yanik, Halil
Celikaslan, Nurgul
Yildirim, Gokhan
Ceylan, Yavuz
author_sort Aslan, Halil
collection PubMed
description BACKGROUND: Caudal regression is a rare syndrome which has a spectrum of congenital malformations ranging from simple anal atresia to absence of sacral, lumbar and possibly lower thoracic vertebrae, to the most severe form which is known as sirenomelia. Maternal diabetes, genetic predisposition and vascular hypoperfusion have been suggested as possible causative factors. CASE PRESENTATION: We report a case of caudal regression syndrome diagnosed in utero at 22 weeks' of gestation. Prenatal ultrasound examination revealed a sudden interruption of the spine and "frog-like" position of lower limbs. Termination of pregnancy and autopsy findings confirmed the diagnosis. CONCLUSION: Prenatal ultrasonographic diagnosis of caudal regression syndrome is possible at 22 weeks' of gestation by ultrasound examination.
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spelling pubmed-644942002-01-11 Prenatal diagnosis of Caudal Regression Syndrome : a case report Aslan, Halil Yanik, Halil Celikaslan, Nurgul Yildirim, Gokhan Ceylan, Yavuz BMC Pregnancy Childbirth Case Report BACKGROUND: Caudal regression is a rare syndrome which has a spectrum of congenital malformations ranging from simple anal atresia to absence of sacral, lumbar and possibly lower thoracic vertebrae, to the most severe form which is known as sirenomelia. Maternal diabetes, genetic predisposition and vascular hypoperfusion have been suggested as possible causative factors. CASE PRESENTATION: We report a case of caudal regression syndrome diagnosed in utero at 22 weeks' of gestation. Prenatal ultrasound examination revealed a sudden interruption of the spine and "frog-like" position of lower limbs. Termination of pregnancy and autopsy findings confirmed the diagnosis. CONCLUSION: Prenatal ultrasonographic diagnosis of caudal regression syndrome is possible at 22 weeks' of gestation by ultrasound examination. BioMed Central 2001-12-11 /pmc/articles/PMC64494/ /pubmed/11782287 http://dx.doi.org/10.1186/1471-2393-1-8 Text en Copyright © 2001 Aslan et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Case Report
Aslan, Halil
Yanik, Halil
Celikaslan, Nurgul
Yildirim, Gokhan
Ceylan, Yavuz
Prenatal diagnosis of Caudal Regression Syndrome : a case report
title Prenatal diagnosis of Caudal Regression Syndrome : a case report
title_full Prenatal diagnosis of Caudal Regression Syndrome : a case report
title_fullStr Prenatal diagnosis of Caudal Regression Syndrome : a case report
title_full_unstemmed Prenatal diagnosis of Caudal Regression Syndrome : a case report
title_short Prenatal diagnosis of Caudal Regression Syndrome : a case report
title_sort prenatal diagnosis of caudal regression syndrome : a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC64494/
https://www.ncbi.nlm.nih.gov/pubmed/11782287
http://dx.doi.org/10.1186/1471-2393-1-8
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