| pubmed-article:3225824 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:3225824 | lifeskim:mentions | umls-concept:C0022658 | lld:lifeskim |
| pubmed-article:3225824 | lifeskim:mentions | umls-concept:C0017382 | lld:lifeskim |
| pubmed-article:3225824 | lifeskim:mentions | umls-concept:C0027341 | lld:lifeskim |
| pubmed-article:3225824 | lifeskim:mentions | umls-concept:C2720748 | lld:lifeskim |
| pubmed-article:3225824 | pubmed:issue | 10 | lld:pubmed |
| pubmed-article:3225824 | pubmed:dateCreated | 1989-4-6 | lld:pubmed |
| pubmed-article:3225824 | 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. | lld:pubmed |
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| pubmed-article:3225824 | pubmed:language | eng | lld:pubmed |
| pubmed-article:3225824 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:3225824 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:3225824 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:3225824 | pubmed:month | Oct | lld:pubmed |
| pubmed-article:3225824 | pubmed:issn | 0022-2593 | lld:pubmed |
| pubmed-article:3225824 | pubmed:author | pubmed-author:van de... | lld:pubmed |
| pubmed-article:3225824 | pubmed:author | pubmed-author:HogewindB LBL | lld:pubmed |
| pubmed-article:3225824 | pubmed:author | pubmed-author:te SlaaR LRL | lld:pubmed |
| pubmed-article:3225824 | pubmed:author | pubmed-author:LooijB JBJJr | lld:pubmed |
| pubmed-article:3225824 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:3225824 | pubmed:volume | 25 | lld:pubmed |
| pubmed-article:3225824 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:3225824 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:3225824 | pubmed:pagination | 682-6 | lld:pubmed |
| pubmed-article:3225824 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
| pubmed-article:3225824 | pubmed:meshHeading | pubmed-meshheading:3225824-... | lld:pubmed |
| pubmed-article:3225824 | pubmed:meshHeading | pubmed-meshheading:3225824-... | lld:pubmed |
| pubmed-article:3225824 | pubmed:meshHeading | pubmed-meshheading:3225824-... | lld:pubmed |
| pubmed-article:3225824 | pubmed:meshHeading | pubmed-meshheading:3225824-... | lld:pubmed |
| pubmed-article:3225824 | pubmed:meshHeading | pubmed-meshheading:3225824-... | lld:pubmed |
| pubmed-article:3225824 | pubmed:meshHeading | pubmed-meshheading:3225824-... | lld:pubmed |
| pubmed-article:3225824 | pubmed:meshHeading | pubmed-meshheading:3225824-... | lld:pubmed |
| pubmed-article:3225824 | pubmed:meshHeading | pubmed-meshheading:3225824-... | lld:pubmed |
| pubmed-article:3225824 | pubmed:year | 1988 | lld:pubmed |
| pubmed-article:3225824 | pubmed:articleTitle | Genetic counselling in hereditary osteo-onychodysplasia (HOOD, nail-patella syndrome) with nephropathy. | lld:pubmed |
| pubmed-article:3225824 | pubmed:affiliation | Department of Nephrology, University Hospital, Leiden, The Netherlands. | lld:pubmed |
| pubmed-article:3225824 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:3225824 | pubmed:publicationType | Case Reports | lld:pubmed |
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