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Prenatal Diagnosis of FATCO Syndrome (Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly) with 2D/3D Ultrasonography
Fibular hemimelia is a congenital lower limb anomaly characterized by the partial or complete absence of the fibula. It includes a spectrum ranging from mild fibular hypoplasia to complete fibular aplasia. Although rare in occurrence, it is the most common congenital absence of long bone of the extr...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Georg Thieme Verlag KG
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7561469/ https://www.ncbi.nlm.nih.gov/pubmed/33073167 http://dx.doi.org/10.1055/a-1225-4388 |
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author | Izadi, Meisam Salehnia, Nasim |
author_facet | Izadi, Meisam Salehnia, Nasim |
author_sort | Izadi, Meisam |
collection | PubMed |
description | Fibular hemimelia is a congenital lower limb anomaly characterized by the partial or complete absence of the fibula. It includes a spectrum ranging from mild fibular hypoplasia to complete fibular aplasia. Although rare in occurrence, it is the most common congenital absence of long bone of the extremities 1 . |
format | Online Article Text |
id | pubmed-7561469 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Georg Thieme Verlag KG |
record_format | MEDLINE/PubMed |
spelling | pubmed-75614692020-10-16 Prenatal Diagnosis of FATCO Syndrome (Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly) with 2D/3D Ultrasonography Izadi, Meisam Salehnia, Nasim Ultrasound Int Open Fibular hemimelia is a congenital lower limb anomaly characterized by the partial or complete absence of the fibula. It includes a spectrum ranging from mild fibular hypoplasia to complete fibular aplasia. Although rare in occurrence, it is the most common congenital absence of long bone of the extremities 1 . Georg Thieme Verlag KG 2020-09 2020-10-15 /pmc/articles/PMC7561469/ /pubmed/33073167 http://dx.doi.org/10.1055/a-1225-4388 Text en The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/). https://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited. |
spellingShingle | Izadi, Meisam Salehnia, Nasim Prenatal Diagnosis of FATCO Syndrome (Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly) with 2D/3D Ultrasonography |
title | Prenatal Diagnosis of FATCO Syndrome (Fibular Aplasia, Tibial
Campomelia, and Oligosyndactyly) with 2D/3D Ultrasonography |
title_full | Prenatal Diagnosis of FATCO Syndrome (Fibular Aplasia, Tibial
Campomelia, and Oligosyndactyly) with 2D/3D Ultrasonography |
title_fullStr | Prenatal Diagnosis of FATCO Syndrome (Fibular Aplasia, Tibial
Campomelia, and Oligosyndactyly) with 2D/3D Ultrasonography |
title_full_unstemmed | Prenatal Diagnosis of FATCO Syndrome (Fibular Aplasia, Tibial
Campomelia, and Oligosyndactyly) with 2D/3D Ultrasonography |
title_short | Prenatal Diagnosis of FATCO Syndrome (Fibular Aplasia, Tibial
Campomelia, and Oligosyndactyly) with 2D/3D Ultrasonography |
title_sort | prenatal diagnosis of fatco syndrome (fibular aplasia, tibial
campomelia, and oligosyndactyly) with 2d/3d ultrasonography |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7561469/ https://www.ncbi.nlm.nih.gov/pubmed/33073167 http://dx.doi.org/10.1055/a-1225-4388 |
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