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- Q574741 subject Q5881496.
- Q574741 subject Q6500135.
- Q574741 subject Q6853484.
- Q574741 subject Q6902466.
- Q574741 subject Q8482266.
- Q574741 abstract "Dubowitz syndrome is a rare genetic disorder characterized by microcephaly, growth retardation and a characteristic facial appearance (small, round, triangular shaped with a pointed, receding chin, a broad, wide-tipped nose, and wide-set eyes with drooping eyelids). Symptoms vary among patients, but other characteristics include a soft, high pitched voice; partial webbing of fingers and toes; palate deformations; genital abnormalities; eczema; hyperactivity; preference for concrete thinking over abstract; language difficulties and aversion to crowds. The pathogenesis of the disease is yet to be identified and no medical tests can definitively diagnose the disease. The main method of diagnosis is through identification of facial phenotype. Since it was first described in 1965 by English physician Victor Dubowitz, over 140 cases have been reported worldwide. Although the majority of cases have been reported from the United States, Germany and Russia, the disorder appears to affect both genders and all ethnicities equally.".
- Q574741 icd10 "Q87.1".
- Q574741 omim "223370".
- Q574741 thumbnail Dubowitz_syndrome_patient.png?width=300.
- Q574741 wikiPageWikiLink Q104053.
- Q574741 wikiPageWikiLink Q1258433.
- Q574741 wikiPageWikiLink Q156871.
- Q574741 wikiPageWikiLink Q159979.
- Q574741 wikiPageWikiLink Q164386.
- Q574741 wikiPageWikiLink Q169872.
- Q574741 wikiPageWikiLink Q17002116.
- Q574741 wikiPageWikiLink Q190199.
- Q574741 wikiPageWikiLink Q191835.
- Q574741 wikiPageWikiLink Q223851.
- Q574741 wikiPageWikiLink Q229256.
- Q574741 wikiPageWikiLink Q28962.
- Q574741 wikiPageWikiLink Q37748.
- Q574741 wikiPageWikiLink Q431643.
- Q574741 wikiPageWikiLink Q43656.
- Q574741 wikiPageWikiLink Q5881496.
- Q574741 wikiPageWikiLink Q6500135.
- Q574741 wikiPageWikiLink Q6531938.
- Q574741 wikiPageWikiLink Q6853484.
- Q574741 wikiPageWikiLink Q6902466.
- Q574741 wikiPageWikiLink Q7208.
- Q574741 wikiPageWikiLink Q75839.
- Q574741 wikiPageWikiLink Q774347.
- Q574741 wikiPageWikiLink Q776995.
- Q574741 wikiPageWikiLink Q7925867.
- Q574741 wikiPageWikiLink Q8482266.
- Q574741 wikiPageWikiLink Q998273.
- Q574741 icd "Q87.1".
- Q574741 name "Dubowitz syndrome".
- Q574741 omim "223370".
- Q574741 type Disease.
- Q574741 type Thing.
- Q574741 type Q12136.
- Q574741 comment "Dubowitz syndrome is a rare genetic disorder characterized by microcephaly, growth retardation and a characteristic facial appearance (small, round, triangular shaped with a pointed, receding chin, a broad, wide-tipped nose, and wide-set eyes with drooping eyelids).".
- Q574741 label "Dubowitz syndrome".
- Q574741 depiction Dubowitz_syndrome_patient.png.
- Q574741 name "Dubowitz syndrome".