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Results 1 - 7 of 7 for Dent disease 1
  1. ... rare condition, with about 250 affected families reported. Dent disease 1 is more common than Dent disease 2.Dent ... OCRL gene. Mutations in the CLCN5 gene cause Dent disease 1, which accounts for about 60 percent of all ...
  2. ... review of aetiology, pathogenesis, diagnosis and management. Aust Dent J. 2010 Jun;55 Suppl 1:39-47. doi: 10.1111/j.1834-7819.2010.01197.x. Citation on PubMed de Paiva CS, Pflugfelder SC. Mechanisms of Disease in Sjogren Syndrome-New Developments and Directions. Int ...
  3. ... 11. doi: 10.1177/154405910808701217. Erratum In: J Dent Res. 2009 Jan;88(1):95. ... of normal variation and disease-causing mutations in the human DSPP gene. Hum ...
  4. ... This form of the condition is often called Dent disease. Like the PHEX gene, the gene associated with Dent disease is located on the X chromosome. In males, ...
  5. ... report and review of the literature. Int J Dent Hyg. 2010 Feb;8(1):68-74. doi: 10.1111/j.1601-5037. ...
  6. ... Organization for Rare Disorders (NORD) WHITE SPONGE NEVUS 1; WSN1 WHITE SPONGE NEVUS 2; WSN2 PubMed Aghbali A, Pouralibaba F, Eslami H, Pakdel F, Jamali Z. White sponge nevus: a case report. J Dent Res Dent Clin Dent Prospects. 2009 Spring;3( ...
  7. ... A review with two case reports. Contemp Clin Dent. 2015 Apr-Jun;6(2):233-6. doi: ... and molecular study of the extracellular matrix protein 1 gene in a spanish family with lipoid proteinosis. ...