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Dent disease 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 ...
- ... 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 ...
- ... 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 ...
- ... 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, ...
- ... report and review of the literature. Int J Dent Hyg. 2010 Feb;8(1):68-74. doi: 10.1111/j.1601-5037. ...
- ... 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( ...
- ... 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. ...