Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q618246> ?p ?o }
Showing triples 1 to 71 of
71
with 100 triples per page.
- Q618246 subject Q6500135.
- Q618246 subject Q6853484.
- Q618246 subject Q7022834.
- Q618246 subject Q7215483.
- Q618246 subject Q8413581.
- Q618246 abstract "Apert syndrome is a form of acrocephalosyndactyly, a congenital disorder characterized by malformations of the skull, face, hands and feet. It is classified as a branchial arch syndrome, affecting the first branchial (or pharyngeal) arch, the precursor of the maxilla and mandible. Disturbances in the development of the branchial arches in fetal development create lasting and widespread effects.In 1906, Eugène Apert, a French physician, described nine people sharing similar attributes and characteristics. Linguistically, "acro" is Greek for "peak", referring to the "peaked" head that is common in the syndrome. "Cephalo", also from Greek, is a combining form meaning "head". "Syndactyly" refers to webbing of fingers and toes.In embryology, the hands and feet have selective cells that die, called selective cell death or apoptosis, causing separation of the digits. In the case of acrocephalosyndactyly, selective cell death does not occur and skin, and rarely bone, between the fingers and toes fuses.The cranial bones are affected as well, similar to Crouzon syndrome and Pfeiffer syndrome. Craniosynostosis occurs when the fetal skull and facial bones fuse too soon in utero, disrupting normal bone growth. Fusion of different sutures leads to different patterns of growth on the skull. Examples include: trigonocephaly (fusion of the metopic suture), brachycephaly (fusion of the coronal suture and lambdoid suture bilaterally), dolichocephaly (fusion of the sagittal suture), plagiocephaly (fusion of coronal and lambdoidal sutures unilaterally), and oxycephaly or turricephaly (fusion of coronal and lambdoid sutures).Findings for the incidence of the syndrome in the population have varied, with estimates as low as 1 birth in 200,000 provided and 160,000 given as an average by older studies. A study conducted in 1997, however, by the California Birth Defects Monitoring Program, found an incidence rate of 1 in 80,645 out of almost 2.5 million live births. Another study conducted in 2002 by the Craniofacial Center, North Texas Hospital For Children, found a higher incidence of about 1 in 65,000 live births.".
- Q618246 icd10 "Q87.0".
- Q618246 icd9 "755.55".
- Q618246 meshId "D000168".
- Q618246 omim "101200".
- Q618246 wikiPageExternalLink apert.htm.
- Q618246 wikiPageExternalLink www.cleftadvocate.org.
- Q618246 wikiPageExternalLink Apert.htm.
- Q618246 wikiPageExternalLink art.asp?articlekey=6574.
- Q618246 wikiPageExternalLink br.fcgi?book=gene&part=craniosynostosis.
- Q618246 wikiPageExternalLink apert-syndrome.
- Q618246 wikiPageWikiLink Q1286848.
- Q618246 wikiPageWikiLink Q131683.
- Q618246 wikiPageWikiLink Q1360044.
- Q618246 wikiPageWikiLink Q1415380.
- Q618246 wikiPageWikiLink Q14599311.
- Q618246 wikiPageWikiLink Q14911644.
- Q618246 wikiPageWikiLink Q1521567.
- Q618246 wikiPageWikiLink Q17148674.
- Q618246 wikiPageWikiLink Q1722542.
- Q618246 wikiPageWikiLink Q1760294.
- Q618246 wikiPageWikiLink Q1774721.
- Q618246 wikiPageWikiLink Q1786496.
- Q618246 wikiPageWikiLink Q182895.
- Q618246 wikiPageWikiLink Q1968264.
- Q618246 wikiPageWikiLink Q2353265.
- Q618246 wikiPageWikiLink Q2546232.
- Q618246 wikiPageWikiLink Q259368.
- Q618246 wikiPageWikiLink Q3059700.
- Q618246 wikiPageWikiLink Q32838.
- Q618246 wikiPageWikiLink Q3508686.
- Q618246 wikiPageWikiLink Q3621760.
- Q618246 wikiPageWikiLink Q378183.
- Q618246 wikiPageWikiLink Q396833.
- Q618246 wikiPageWikiLink Q42649.
- Q618246 wikiPageWikiLink Q427157.
- Q618246 wikiPageWikiLink Q5283631.
- Q618246 wikiPageWikiLink Q5691660.
- Q618246 wikiPageWikiLink Q609809.
- Q618246 wikiPageWikiLink Q6500135.
- Q618246 wikiPageWikiLink Q6531938.
- Q618246 wikiPageWikiLink Q6853484.
- Q618246 wikiPageWikiLink Q7020.
- Q618246 wikiPageWikiLink Q7022834.
- Q618246 wikiPageWikiLink Q7187.
- Q618246 wikiPageWikiLink Q7215483.
- Q618246 wikiPageWikiLink Q727096.
- Q618246 wikiPageWikiLink Q748758.
- Q618246 wikiPageWikiLink Q775482.
- Q618246 wikiPageWikiLink Q775497.
- Q618246 wikiPageWikiLink Q779250.
- Q618246 wikiPageWikiLink Q832528.
- Q618246 wikiPageWikiLink Q840737.
- Q618246 wikiPageWikiLink Q8413581.
- Q618246 wikiPageWikiLink Q917177.
- Q618246 icd "755.55".
- Q618246 icd "Q87.0".
- Q618246 meshid "D000168".
- Q618246 name "Apert syndrome".
- Q618246 omim "101200".
- Q618246 type Disease.
- Q618246 type Thing.
- Q618246 type Q12136.
- Q618246 comment "Apert syndrome is a form of acrocephalosyndactyly, a congenital disorder characterized by malformations of the skull, face, hands and feet. It is classified as a branchial arch syndrome, affecting the first branchial (or pharyngeal) arch, the precursor of the maxilla and mandible.".
- Q618246 label "Apert syndrome".
- Q618246 name "Apert syndrome".