Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion Syndrome.
Masatake ToshimitsuShinichi NagaokaShuusaku KoboriMaki OgawaFumihiko SuzukiTakema KatoShunsuke MiyaiRie KawamuraHidehito InagakiHiroki KurahashiJun MurotsukiPublished in: Case reports in obstetrics and gynecology (2019)
Using the exome-first approach, we identified a case with fetal akinesia associated with chromosome 1p36 deletion. Chromosome 1p36 deletion syndrome may be considered for differential diagnosis in cases of fetal akinesia with multiple abnormalities.