Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q3508774> ?p ?o }
Showing triples 1 to 25 of
25
with 100 triples per page.
- Q3508774 subject Q6500135.
- Q3508774 subject Q6853484.
- Q3508774 subject Q6902466.
- Q3508774 subject Q7031586.
- Q3508774 subject Q8795300.
- Q3508774 abstract "Wiedemann–Rautenstrauch (WR) syndrome [ˈviːdəman ˈʁa͜ʊtən.ʃtʁa͜ʊx], also known as neonatal progeroid syndrome, is an autosomal recessive progeroid syndrome.WR was first reported by Rautenstrauch and Snigula in 1977; and the earliest reports made subsequently have been by Wiedemann in 1979, by Devos in 1981, and Rudin in 1988. There has been over 30 cases of WR.WR is associated with abnormalities in bone maturation, and lipids and hormone metabolism. Affected individuals exhibit intrauterine and postnatal growth retardation, leading to short stature and an aged appearance from birth. They have physical abnormalities including a large head (macrocephaly), sparse hair, prominent scalp veins, inward-folded eyelid (entropion), widened anterior fontanelles, hollow cheeks (malar hypoplasia), general loss of fat tissues under the skin (lipoatrophy), delayed tooth eruption, abnormal hair pattern (hypotrichosis), beaked nose, mild to severe mental retardation and dysmorphism.".
- Q3508774 icd10 "E34.8".
- Q3508774 omim "264090".
- Q3508774 wikiPageWikiLink Q1269290.
- Q3508774 wikiPageWikiLink Q1641483.
- Q3508774 wikiPageWikiLink Q6139748.
- Q3508774 wikiPageWikiLink Q6500135.
- Q3508774 wikiPageWikiLink Q6853484.
- Q3508774 wikiPageWikiLink Q6902466.
- Q3508774 wikiPageWikiLink Q7031586.
- Q3508774 wikiPageWikiLink Q8795300.
- Q3508774 icd "E34.8".
- Q3508774 name "Wiedemann–Rautenstrauch syndrome".
- Q3508774 omim "264090".
- Q3508774 type Disease.
- Q3508774 type Thing.
- Q3508774 type Q12136.
- Q3508774 comment "Wiedemann–Rautenstrauch (WR) syndrome [ˈviːdəman ˈʁa͜ʊtən.ʃtʁa͜ʊx], also known as neonatal progeroid syndrome, is an autosomal recessive progeroid syndrome.WR was first reported by Rautenstrauch and Snigula in 1977; and the earliest reports made subsequently have been by Wiedemann in 1979, by Devos in 1981, and Rudin in 1988. There has been over 30 cases of WR.WR is associated with abnormalities in bone maturation, and lipids and hormone metabolism.".
- Q3508774 label "Wiedemann–Rautenstrauch syndrome".
- Q3508774 name "Wiedemann–Rautenstrauch syndrome".