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Decreased fetal movement prompts investigation of prenatal/neonatal nemaline myopathy: The possible merit of fetal movement count
Author(s) -
Kuwata Tomoyuki,
Matsubara Shigeki,
Ohkusa Takashi,
Yada Yukari,
Suzuki Mitsuaki
Publication year - 2011
Publication title -
journal of obstetrics and gynaecology research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.597
H-Index - 50
eISSN - 1447-0756
pISSN - 1341-8076
DOI - 10.1111/j.1447-0756.2010.01438.x
Subject(s) - medicine , nemaline myopathy , fetal movement , myopathy , fetus , movement (music) , obstetrics , pregnancy , physics , biology , genetics , acoustics
We highlight the merit of fetal movement count to identify a fetus with neuromuscular disorder: nemaline myopathy. A 38‐year‐old 1‐para woman not in a consanguineous marriage had decreased fetal movement. This, together with increased amniotic fluid volume, led us to perform detailed ultrasound examinations, which revealed stretch contracture of the knee joints, leading us to suspect fetal neuromuscular disorders. At 38 2/7 , she gave birth vaginally to a 2444 g female infant. Her respiration was very weak, requiring respiratory support. Contractures of the upper/lower extremity joints and club feet were observed. All skeletal muscles were hypotonic. Biopsized muscle cells showed nemaline bodies, confirming the diagnosis of nemaline myopathy. Fetal movement count may contribute to the identification of fetal neuromuscular diseases, such as nemaline myopathy.