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Prenatal diagnosis of tibial hemimelia type I and omphalocele, a rare entity and postnatal correlation

Hemimelia is a rare anomaly affecting the distal long bones of extremities, with an occurrence of 1–20 cases per million of live births depending on the affected bone. Hemimelia can be an isolated defect or be part of complex syndromes that affect extra skeletal structures. Prenatal detection by rou...

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Detalles Bibliográficos
Autores principales: Molina-Giraldo, Saulo, Saucedo, Jesus Armando, Navarro-Devia, Antonio José, Buitrago-Leal, Marcela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The British Institute of Radiology. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7869132/
https://www.ncbi.nlm.nih.gov/pubmed/33614110
http://dx.doi.org/10.1259/bjrcr.20200002
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author Molina-Giraldo, Saulo
Saucedo, Jesus Armando
Navarro-Devia, Antonio José
Buitrago-Leal, Marcela
author_facet Molina-Giraldo, Saulo
Saucedo, Jesus Armando
Navarro-Devia, Antonio José
Buitrago-Leal, Marcela
author_sort Molina-Giraldo, Saulo
collection PubMed
description Hemimelia is a rare anomaly affecting the distal long bones of extremities, with an occurrence of 1–20 cases per million of live births depending on the affected bone. Hemimelia can be an isolated defect or be part of complex syndromes that affect extra skeletal structures. Prenatal detection by routine ultrasound imaging is difficult and yields low detection rates. The prenatal diagnosis of hemimelia should prompt a complete and detailed study of the fetal anatomy, since it can be associated with defects in other structures and systems, as the reported in this case. The prognosis depends upon the associated anomalies.
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spelling pubmed-78691322021-02-19 Prenatal diagnosis of tibial hemimelia type I and omphalocele, a rare entity and postnatal correlation Molina-Giraldo, Saulo Saucedo, Jesus Armando Navarro-Devia, Antonio José Buitrago-Leal, Marcela BJR Case Rep Case Report Hemimelia is a rare anomaly affecting the distal long bones of extremities, with an occurrence of 1–20 cases per million of live births depending on the affected bone. Hemimelia can be an isolated defect or be part of complex syndromes that affect extra skeletal structures. Prenatal detection by routine ultrasound imaging is difficult and yields low detection rates. The prenatal diagnosis of hemimelia should prompt a complete and detailed study of the fetal anatomy, since it can be associated with defects in other structures and systems, as the reported in this case. The prognosis depends upon the associated anomalies. The British Institute of Radiology. 2020-09-04 /pmc/articles/PMC7869132/ /pubmed/33614110 http://dx.doi.org/10.1259/bjrcr.20200002 Text en © 2021 The Authors. Published by the British Institute of Radiology This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
spellingShingle Case Report
Molina-Giraldo, Saulo
Saucedo, Jesus Armando
Navarro-Devia, Antonio José
Buitrago-Leal, Marcela
Prenatal diagnosis of tibial hemimelia type I and omphalocele, a rare entity and postnatal correlation
title Prenatal diagnosis of tibial hemimelia type I and omphalocele, a rare entity and postnatal correlation
title_full Prenatal diagnosis of tibial hemimelia type I and omphalocele, a rare entity and postnatal correlation
title_fullStr Prenatal diagnosis of tibial hemimelia type I and omphalocele, a rare entity and postnatal correlation
title_full_unstemmed Prenatal diagnosis of tibial hemimelia type I and omphalocele, a rare entity and postnatal correlation
title_short Prenatal diagnosis of tibial hemimelia type I and omphalocele, a rare entity and postnatal correlation
title_sort prenatal diagnosis of tibial hemimelia type i and omphalocele, a rare entity and postnatal correlation
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7869132/
https://www.ncbi.nlm.nih.gov/pubmed/33614110
http://dx.doi.org/10.1259/bjrcr.20200002
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