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Antenatal Indomethacin Treatment for Congenital Myotonic Dystrophy

Myotonic dystrophy is an autosomal-dominant disorder. Its congenital type is the most severe form, with respiratory failure that can be a life-threatening event after birth. There are no antenatal treatments that can improve neonatal outcomes of myotonic dystrophy. We treated a fetus with congenital...

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Autores principales: Yamaguchi, Kyohei, Tanaka, Hiroaki, Furuhashi, Fumi H., Tanaka, Kayo, Kondo, Eiji, Ikeda, Tomoaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393864/
https://www.ncbi.nlm.nih.gov/pubmed/30906607
http://dx.doi.org/10.1155/2019/4290145
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author Yamaguchi, Kyohei
Tanaka, Hiroaki
Furuhashi, Fumi H.
Tanaka, Kayo
Kondo, Eiji
Ikeda, Tomoaki
author_facet Yamaguchi, Kyohei
Tanaka, Hiroaki
Furuhashi, Fumi H.
Tanaka, Kayo
Kondo, Eiji
Ikeda, Tomoaki
author_sort Yamaguchi, Kyohei
collection PubMed
description Myotonic dystrophy is an autosomal-dominant disorder. Its congenital type is the most severe form, with respiratory failure that can be a life-threatening event after birth. There are no antenatal treatments that can improve neonatal outcomes of myotonic dystrophy. We treated a fetus with congenital myotonic dystrophy by administering indomethacin to the 31-year-old Japanese mother affected by myotonic dystrophy and polyhydramnios. We observed increased fetal breathing movement and a reduction of the amniotic fluid volume. The baby was born at 37 weeks and discharged from the neonatal intensive care unit with a favorable outcome. Indomethacin treatment is likely to improve fetal lung function and to control the amniotic fluid volume. This report emphasizes the importance of further investigations regarding the optimal management of congenital myotonic dystrophy.
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spelling pubmed-63938642019-03-24 Antenatal Indomethacin Treatment for Congenital Myotonic Dystrophy Yamaguchi, Kyohei Tanaka, Hiroaki Furuhashi, Fumi H. Tanaka, Kayo Kondo, Eiji Ikeda, Tomoaki Case Rep Obstet Gynecol Case Report Myotonic dystrophy is an autosomal-dominant disorder. Its congenital type is the most severe form, with respiratory failure that can be a life-threatening event after birth. There are no antenatal treatments that can improve neonatal outcomes of myotonic dystrophy. We treated a fetus with congenital myotonic dystrophy by administering indomethacin to the 31-year-old Japanese mother affected by myotonic dystrophy and polyhydramnios. We observed increased fetal breathing movement and a reduction of the amniotic fluid volume. The baby was born at 37 weeks and discharged from the neonatal intensive care unit with a favorable outcome. Indomethacin treatment is likely to improve fetal lung function and to control the amniotic fluid volume. This report emphasizes the importance of further investigations regarding the optimal management of congenital myotonic dystrophy. Hindawi 2019-02-14 /pmc/articles/PMC6393864/ /pubmed/30906607 http://dx.doi.org/10.1155/2019/4290145 Text en Copyright © 2019 Kyohei Yamaguchi et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Yamaguchi, Kyohei
Tanaka, Hiroaki
Furuhashi, Fumi H.
Tanaka, Kayo
Kondo, Eiji
Ikeda, Tomoaki
Antenatal Indomethacin Treatment for Congenital Myotonic Dystrophy
title Antenatal Indomethacin Treatment for Congenital Myotonic Dystrophy
title_full Antenatal Indomethacin Treatment for Congenital Myotonic Dystrophy
title_fullStr Antenatal Indomethacin Treatment for Congenital Myotonic Dystrophy
title_full_unstemmed Antenatal Indomethacin Treatment for Congenital Myotonic Dystrophy
title_short Antenatal Indomethacin Treatment for Congenital Myotonic Dystrophy
title_sort antenatal indomethacin treatment for congenital myotonic dystrophy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393864/
https://www.ncbi.nlm.nih.gov/pubmed/30906607
http://dx.doi.org/10.1155/2019/4290145
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