Kétoldali veseagenesia családi elöfordulása.

Translated title of the contribution: Familial occurrence of bilateral renal agenesis

T. Kovács, K. Csécsei, Z. Tóth, Z. Papp

Research output: Contribution to journalArticle

Abstract

The 58 cases of bilateral renal agenesis (Potter syndrome) registered in the Genetic Counselling of our institute in the last 12 years are reviewed. The only recurrent case which has been prenatally diagnosed is described in details. An urinary bladder anomaly like that of the subsequent child has not been reported in such a family previously. The authors analyze the possible inheritance patterns taking into account the previous references, too. They suggest the malformation is a genetically heterogeneous entity. They emphasize that nowadays the birth of a newborn with bilateral renal agenesis can be prevented in all cases.

Translated title of the contributionFamilial occurrence of bilateral renal agenesis
Original languageHungarian
Pages (from-to)133-135
Number of pages3
JournalOrvosi hetilap
Volume131
Issue number3
Publication statusPublished - Jan 21 1990

ASJC Scopus subject areas

  • Medicine(all)

Fingerprint Dive into the research topics of 'Familial occurrence of bilateral renal agenesis'. Together they form a unique fingerprint.

  • Cite this

    Kovács, T., Csécsei, K., Tóth, Z., & Papp, Z. (1990). Kétoldali veseagenesia családi elöfordulása. Orvosi hetilap, 131(3), 133-135.