Abstract
Rationale:Sirenomelia and anencephaly are well-defined congenital malformations that usually occur independently.Patient concerns:We report a case of combined sirenomelia, anencephaly and complete rachischisis, diagnosed in the 16th week of gestation.Diagnoses:To our knowledge, this is the 7th case in the literature and the first that is diagnosed so early in pregnancy.Interventions:The final diagnosis is confirmed with radiological examination after the termination of pregnancy.Outcomes:Prenatal diagnosis of sirenomelia is difficult due to the presence of kidney agenesis and severe oligohydramnios.Lessons:The combination of sirenomelia and craniorachischisis totalis is extremely rare and prenatal ultrasound scan are a challenge, even for experts in the field.
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Theofanakis, C., Theodora, M., Sindos, M., & Daskalakis, G. (2017). Prenatal diagnosis of sirenomelia with anencephaly and craniorachischisis totalis: A case report study. Medicine (United States), 96(50). https://doi.org/10.1097/MD.0000000000009020
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