Prenatal diagnosis and treatment for fetal angiotensin converting enzyme deficiency
To elucidate an etiology in a case with persistent oligohydramnios by prenatal diagnosis and actively treat the case to achieve good prognosis. We performed whole exome sequencing (WES) of DNA from the fetus and parents. Serial amnioinfusions were conducted until birth. Pressors were required to mai...
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Veröffentlicht in: | Prenatal diagnosis 2024-02, Vol.44 (2), p.167-171 |
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Sprache: | eng |
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