Autoszóm domináns öröklödésü polycystás vesebetegség I. típusának magzati géndiagnosztikája.

Translated title of the contribution: Prenatal genetic diagnosis of type I autosomal dominant polycystic kidney disease

Z. Klaus, M. Kozáry, E. Czeizel

Research output: Contribution to journalArticle

Abstract

Probanda affected with autosomal dominant polycystic kidney disease (ADPKD) had a molecular genetic analysis which indicated the type I. Of the three pregnancies in the probanda, first two had mutant gene carrier fetuses and these pregnancies were terminated. The fetus of the third pregnancy had no mutant gene and this pregnancy ended in the birth of a healthy boy. The principles of genetic counselling and antenatal care are summarised in ADPKD type I.

Original languageHungarian
Pages (from-to)1571-1574
Number of pages4
JournalOrvosi Hetilap
Volume138
Issue number24
Publication statusPublished - Jun 15 1997

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Autosomal Dominant Polycystic Kidney
Prenatal Diagnosis
Pregnancy
Fetus
Prenatal Care
Genetic Counseling
Genes
Molecular Biology
Parturition

ASJC Scopus subject areas

  • Medicine(all)

Cite this

Autoszóm domináns öröklödésü polycystás vesebetegség I. típusának magzati géndiagnosztikája. / Klaus, Z.; Kozáry, M.; Czeizel, E.

In: Orvosi Hetilap, Vol. 138, No. 24, 15.06.1997, p. 1571-1574.

Research output: Contribution to journalArticle

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