Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q17156923> ?p ?o }
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- Q17156923 subject Q5881496.
- Q17156923 subject Q6193293.
- Q17156923 subject Q8672800.
- Q17156923 abstract "Sepiapterin reductase deficiency is an inherited pediatric disorder characterized by movement problems, and most commonly displayed as a pattern of involuntary sustained muscle contractions known as dystonia. Symptoms are usually present within the first year of age, but diagnosis is delayed due to physicians lack of awareness and the specialized diagnostic procedures. Individuals with this disorder also have delayed motor skills development including sitting, crawling, and need assistance when walking. Additional symptoms of this disorder include intellectual disability, excessive sleeping, mood swings, and an abnormally small head size. SR deficiency is a very rare condition. The first case was diagnosed in 2001, and since then there have been approximately 30 reported cases. At this time, the condition seems to be treatable, but due to a lack of overall awareness and a series of atypical procedures used to diagnose this condition pose a dilemma.".
- Q17156923 wikiPageExternalLink sepiapterin-reductase-deficiency.
- Q17156923 wikiPageExternalLink SPR.htm.
- Q17156923 wikiPageExternalLink Sepiapterin_reductase_deficiency.aspx.
- Q17156923 wikiPageExternalLink CHILDx%202009%20Hyland.pdf.
- Q17156923 wikiPageExternalLink What_Are_PNDs.htm.
- Q17156923 wikiPageWikiLink Q104053.
- Q17156923 wikiPageWikiLink Q11085.
- Q17156923 wikiPageWikiLink Q13048280.
- Q17156923 wikiPageWikiLink Q1415380.
- Q17156923 wikiPageWikiLink Q1531991.
- Q17156923 wikiPageWikiLink Q15331000.
- Q17156923 wikiPageWikiLink Q162657.
- Q17156923 wikiPageWikiLink Q167934.
- Q17156923 wikiPageWikiLink Q170304.
- Q17156923 wikiPageWikiLink Q1753547.
- Q17156923 wikiPageWikiLink Q18254977.
- Q17156923 wikiPageWikiLink Q210427.
- Q17156923 wikiPageWikiLink Q211083.
- Q17156923 wikiPageWikiLink Q213373.
- Q17156923 wikiPageWikiLink Q21608541.
- Q17156923 wikiPageWikiLink Q225957.
- Q17156923 wikiPageWikiLink Q2823333.
- Q17156923 wikiPageWikiLink Q28745.
- Q17156923 wikiPageWikiLink Q300989.
- Q17156923 wikiPageWikiLink Q373027.
- Q17156923 wikiPageWikiLink Q386702.
- Q17156923 wikiPageWikiLink Q408256.
- Q17156923 wikiPageWikiLink Q414225.
- Q17156923 wikiPageWikiLink Q419808.
- Q17156923 wikiPageWikiLink Q424455.
- Q17156923 wikiPageWikiLink Q4333327.
- Q17156923 wikiPageWikiLink Q463418.
- Q17156923 wikiPageWikiLink Q54196.
- Q17156923 wikiPageWikiLink Q5420592.
- Q17156923 wikiPageWikiLink Q5881496.
- Q17156923 wikiPageWikiLink Q6193293.
- Q17156923 wikiPageWikiLink Q6531938.
- Q17156923 wikiPageWikiLink Q7020.
- Q17156923 wikiPageWikiLink Q7094.
- Q17156923 wikiPageWikiLink Q742500.
- Q17156923 wikiPageWikiLink Q8047.
- Q17156923 wikiPageWikiLink Q8672800.
- Q17156923 wikiPageWikiLink Q903566.
- Q17156923 wikiPageWikiLink Q906492.
- Q17156923 wikiPageWikiLink Q908292.
- Q17156923 comment "Sepiapterin reductase deficiency is an inherited pediatric disorder characterized by movement problems, and most commonly displayed as a pattern of involuntary sustained muscle contractions known as dystonia. Symptoms are usually present within the first year of age, but diagnosis is delayed due to physicians lack of awareness and the specialized diagnostic procedures.".
- Q17156923 label "Sepiapterin reductase deficiency".