Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
1989-4-6
pubmed:abstractText
Hereditary osteo-onychodysplasia (HOOD, nail-patella syndrome) is an autosomal dominant condition characterised by nail dysplasia, patellar hypoplasia or aplasia, and nephropathy. The risk for HOOD patients to have a child with HOOD who will develop renal failure cannot easily be deduced from published pedigrees. We have studied a large family with 30 patients with HOOD and have analysed 34 kindreds with HOOD nephropathy from published reports, comprising 213 patients. For a patient with HOOD from a family in which HOOD nephropathy occurs, the risk of having a child with HOOD nephropathy is about 1:4; the risk of having a child in whom renal failure will develop is about 1:10.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-13314404, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-14081557, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-14206765, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-14295509, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-14304642, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-14388536, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-15416035, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-15419189, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-184030, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-4032839, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-4334458, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-4470908, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-4568821, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-4569963, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-4571998, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-4575683, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-4641021, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-4682988, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-4693887, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-5110573, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-5365763, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-5423458, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-552687, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-5778286, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-5790679, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-5945537, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-6019383, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-6028699, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-609821, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-6162320, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-6507504, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-713167, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-7158631, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-7343113, http://linkedlifedata.com/resource/pubmed/commentcorrection/3225824-894783
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0022-2593
pubmed:author
pubmed:issnType
Print
pubmed:volume
25
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
682-6
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1988
pubmed:articleTitle
Genetic counselling in hereditary osteo-onychodysplasia (HOOD, nail-patella syndrome) with nephropathy.
pubmed:affiliation
Department of Nephrology, University Hospital, Leiden, The Netherlands.
pubmed:publicationType
Journal Article, Case Reports