Prenatal genetic diagnosis of disseminated infantile myofibromatosis: a case report and literature review
Abstract Background Infantile myofibromatosis (IM) is a rare disorder characterized by the formation of nodules in the skin, muscle, bone, and, more rarely, visceral organs. Very few cases are detected prenatally, and the final diagnosis cannot be made until pathology is completed after birth. Here,...
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Format: | Book |
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BMC,
2023-08-01T00:00:00Z.
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A1234.567 |
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