Zentralblatt fur Gynakologie · 1999
[Prenatal diagnosis of sirenomelia].
Клинический случайСтатьяНазвание и аннотация: Перевод в очереди
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Tönnies P, Watermann D, Gellén J
Аннотация
OBJECTIVE: What kind of diagnostical methods are usual to detect fetal sirenomelia?
MATERIAL AND METHODS: The prenatal diagnosis of fetal sirenomelia combined with bilateral renal agenesis, oligohydramnios and single umbilical artery in a 24-year-old woman, gravida 2, para 1, at a gestational age of 18 + 3 weeks is described in this case report.
RESULTS: This fetal malformation was an accidental sonographic found, and caused after confirming diagnosis by amnoinfusion and amniocentesis, the termination of pregnancy. Genetic examination revealed tetrasomia 13.
CONCLUSIONS: The sonographic finding of oligohydramnios should cause an exactly sonographical examination with amnioinfusion. In case of sirenomelia genetical examination is necessary.
MATERIAL AND METHODS: The prenatal diagnosis of fetal sirenomelia combined with bilateral renal agenesis, oligohydramnios and single umbilical artery in a 24-year-old woman, gravida 2, para 1, at a gestational age of 18 + 3 weeks is described in this case report.
RESULTS: This fetal malformation was an accidental sonographic found, and caused after confirming diagnosis by amnoinfusion and amniocentesis, the termination of pregnancy. Genetic examination revealed tetrasomia 13.
CONCLUSIONS: The sonographic finding of oligohydramnios should cause an exactly sonographical examination with amnioinfusion. In case of sirenomelia genetical examination is necessary.