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Prenatal diagnosis of sirenomelia with anencephaly and craniorachischisis totalis: A case report study
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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5815709/ https://www.ncbi.nlm.nih.gov/pubmed/29390297 http://dx.doi.org/10.1097/MD.0000000000009020 |
Sumario: | 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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