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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Main Authors: Kyohei Yamaguchi, Hiroaki Tanaka, Fumi H. Furuhashi, Kayo Tanaka, Eiji Kondo, Tomoaki Ikeda
Format: Article
Language:English
Published: Hindawi Limited 2019-01-01
Series:Case Reports in Obstetrics and Gynecology
Online Access:http://dx.doi.org/10.1155/2019/4290145
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spelling doaj-78d7ab85e81241409233d9ca9a22c5bf2020-11-25T00:02:27ZengHindawi LimitedCase Reports in Obstetrics and Gynecology2090-66842090-66922019-01-01201910.1155/2019/42901454290145Antenatal Indomethacin Treatment for Congenital Myotonic DystrophyKyohei Yamaguchi0Hiroaki Tanaka1Fumi H. Furuhashi2Kayo Tanaka3Eiji Kondo4Tomoaki Ikeda5Department of Obstetrics and Gynecology, Mie University, Mie, JapanDepartment of Obstetrics and Gynecology, Mie University, Mie, JapanDepartment of Obstetrics and Gynecology, Mie University, Mie, JapanDepartment of Obstetrics and Gynecology, Mie University, Mie, JapanDepartment of Obstetrics and Gynecology, Mie University, Mie, JapanDepartment of Obstetrics and Gynecology, Mie University, Mie, JapanMyotonic 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.http://dx.doi.org/10.1155/2019/4290145
collection DOAJ
language English
format Article
sources DOAJ
author Kyohei Yamaguchi
Hiroaki Tanaka
Fumi H. Furuhashi
Kayo Tanaka
Eiji Kondo
Tomoaki Ikeda
spellingShingle Kyohei Yamaguchi
Hiroaki Tanaka
Fumi H. Furuhashi
Kayo Tanaka
Eiji Kondo
Tomoaki Ikeda
Antenatal Indomethacin Treatment for Congenital Myotonic Dystrophy
Case Reports in Obstetrics and Gynecology
author_facet Kyohei Yamaguchi
Hiroaki Tanaka
Fumi H. Furuhashi
Kayo Tanaka
Eiji Kondo
Tomoaki Ikeda
author_sort Kyohei Yamaguchi
title Antenatal Indomethacin Treatment for Congenital Myotonic Dystrophy
title_short 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_sort antenatal indomethacin treatment for congenital myotonic dystrophy
publisher Hindawi Limited
series Case Reports in Obstetrics and Gynecology
issn 2090-6684
2090-6692
publishDate 2019-01-01
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.
url http://dx.doi.org/10.1155/2019/4290145
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AT kayotanaka antenatalindomethacintreatmentforcongenitalmyotonicdystrophy
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