Linked Life Data

2300395

Source:http://linkedlifedata.com/resource/pubmed/id/2300395

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1990-3-8
pubmed:abstractText
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.
pubmed:language
hun
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0030-6002
pubmed:author
pubmed:issnType
Print
pubmed:day
21
pubmed:volume
131
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
133-5
pubmed:dateRevised
2009-10-21
pubmed:meshHeading
pubmed:year
1990
pubmed:articleTitle
[Familial occurrence of bilateral renal agenesis].
pubmed:affiliation
Debreceni Orvostudományi Egyetem, Nöi Klinika.
pubmed:publicationType
Journal Article, English Abstract, Case Reports