CareLit · DOI-Nachweis · Ultraschall in der Medizin - European Journal of Ultrasound
Amniocentesis and genetic diagnostic-key points, for prognostic of fetes carrier of cystic fibrosis mutation
DOI 10.1055/s-2008-1079873
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Autor:innenD Albu, D Pelinescu-Onciul
ZeitschriftUltraschall in der Medizin - European Journal of Ultrasound
Ausgabe05/2008
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
We present a case of cystic fibrosis. A secondary gravida referred to our service with a pregnancy of 7 weeks of gestation. Two years ago, she gave birth to a boy with cystic fibrosis. She and her husband were perfect healthy persons. We perform genetic test to both parents and to first child. Parents were heterozygote for DF 508 mutation, and the children homozygote. The chances for this pregnancy were 50% heterozy…
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Zitierempfehlung
D Albu, D Pelinescu-Onciul (2008) Amniocentesis and genetic diagnostic-key points, for prognostic of fetes carrier of cystic fibrosis mutation. Ultraschall in der Medizin - European Journal of Ultrasound (05). https://doi.org/10.1055/s-2008-1079873
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