A carrier with de novo Mutation in the dystrophin gene whose myopathic symptoms became seriously progressive after pregnancy and delivery
Muscle Nerve
.
2015 Nov;52(5):913-4.
doi: 10.1002/mus.24744.
Epub 2015 Jul 24.
Authors
Hiroko Hori
1
,
Yasushi Maeda
1
,
Masatoshi Ishizaki
1
,
Tomoo Hirahara
1
,
Masaki Watanabe
1
,
Satoshi Yamashita
1
,
Taro Yamashita
1
,
Makoto Uchino
1
,
Yukio Ando
1
Affiliation
1
Department of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
PMID:
26088440
DOI:
10.1002/mus.24744
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Adult
Delivery, Obstetric / trends*
Disease Progression*
Dystrophin / genetics*
Female
Heterozygote*
Humans
Muscle Weakness / diagnosis
Muscle Weakness / genetics*
Mutation / genetics*
Pregnancy
Substances
Dystrophin