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Congenital contractural arachnodactyly suspected by abnormally long extremities by fetal ultrasound

Congenital contractural arachnodactyly (CCA) is a rare disease with the clinical features of limited extension of multiple joints, arachnodactyly, camptodactyly, thin and long extremities, and so on. In the point of long extremities, CCA resembles Marfan syndrome (MFS). CCA is easily differentiated...

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Autores principales: Miyake, Ryuta, Ichikawa, Mayuko, Naruse, Katsuhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7929828/
https://www.ncbi.nlm.nih.gov/pubmed/33649036
http://dx.doi.org/10.1136/bcr-2020-237904
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author Miyake, Ryuta
Ichikawa, Mayuko
Naruse, Katsuhiko
author_facet Miyake, Ryuta
Ichikawa, Mayuko
Naruse, Katsuhiko
author_sort Miyake, Ryuta
collection PubMed
description Congenital contractural arachnodactyly (CCA) is a rare disease with the clinical features of limited extension of multiple joints, arachnodactyly, camptodactyly, thin and long extremities, and so on. In the point of long extremities, CCA resembles Marfan syndrome (MFS). CCA is easily differentiated from MFS after birth due to the flexion of multiple joints, including elbows, knees, hips and fingers. During the fetal period, observation of arachnodactyly and folded fingers by fetal ultrasound is the means of differential diagnosis between these two diseases. We report on a case of CCA diagnosed with prenatal symptoms of long extremities, and introduced physiotherapy in early childhood for a better physical prognosis.
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spelling pubmed-79298282021-03-19 Congenital contractural arachnodactyly suspected by abnormally long extremities by fetal ultrasound Miyake, Ryuta Ichikawa, Mayuko Naruse, Katsuhiko BMJ Case Rep Case Report Congenital contractural arachnodactyly (CCA) is a rare disease with the clinical features of limited extension of multiple joints, arachnodactyly, camptodactyly, thin and long extremities, and so on. In the point of long extremities, CCA resembles Marfan syndrome (MFS). CCA is easily differentiated from MFS after birth due to the flexion of multiple joints, including elbows, knees, hips and fingers. During the fetal period, observation of arachnodactyly and folded fingers by fetal ultrasound is the means of differential diagnosis between these two diseases. We report on a case of CCA diagnosed with prenatal symptoms of long extremities, and introduced physiotherapy in early childhood for a better physical prognosis. BMJ Publishing Group 2021-03-01 /pmc/articles/PMC7929828/ /pubmed/33649036 http://dx.doi.org/10.1136/bcr-2020-237904 Text en © BMJ Publishing Group Limited 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Case Report
Miyake, Ryuta
Ichikawa, Mayuko
Naruse, Katsuhiko
Congenital contractural arachnodactyly suspected by abnormally long extremities by fetal ultrasound
title Congenital contractural arachnodactyly suspected by abnormally long extremities by fetal ultrasound
title_full Congenital contractural arachnodactyly suspected by abnormally long extremities by fetal ultrasound
title_fullStr Congenital contractural arachnodactyly suspected by abnormally long extremities by fetal ultrasound
title_full_unstemmed Congenital contractural arachnodactyly suspected by abnormally long extremities by fetal ultrasound
title_short Congenital contractural arachnodactyly suspected by abnormally long extremities by fetal ultrasound
title_sort congenital contractural arachnodactyly suspected by abnormally long extremities by fetal ultrasound
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7929828/
https://www.ncbi.nlm.nih.gov/pubmed/33649036
http://dx.doi.org/10.1136/bcr-2020-237904
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