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Results 1 - 10 of 12 for Dent disease 1
  1. Dent disease 
    ... 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 ...
    https://medlineplus.gov/genetics/condition/dent-disease - Genetics
  2. CLCN5 gene 
    ... the CLCN5 gene have been found to cause Dent disease 1, a chronic kidney disorder that can cause kidney ... stones, and related health problems in people with Dent disease 1. Abnormal proximal tubule function ultimately leads to kidney ...
    https://medlineplus.gov/genetics/gene/clcn5 - Genetics
  3. Sjögren syndrome 
    ... 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 ...
    https://medlineplus.gov/genetics/condition/sjogren-syndrome - Genetics
  4. DSPP gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/dspp - Genetics
  5. Dentinogenesis imperfecta 
    ... 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 ...
    https://medlineplus.gov/genetics/condition/dentinogenesis-imperfecta - Genetics
  6. OCRL gene 
    ... the OCRL gene have been found to cause Dent disease 2. This form of Dent disease is characterized by chronic kidney problems; some affected ... that does not impair vision. Some researchers consider Dent disease 2 to be a mild variant of Lowe ...
    https://medlineplus.gov/genetics/gene/ocrl - Genetics
  7. Hereditary hypophosphatemic rickets 
    ... 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, ...
    https://medlineplus.gov/.../hereditary-hypophosphatemic-rickets - Genetics
  8. DSP gene 
    ... Naxos syndrome secondary to desmoplakin-dominant mutations. J Dent Res. 2011 Jan;90(1):58-64. doi: 10.1177/0022034510383984. Epub 2010 ... desmoplakin mutations in cardiomyopathy patients reveal different molecular disease mechanisms. Clin Genet. 2013 Jul;84(1):20-30. doi: 10.1111/cge.12056. Epub ...
    https://medlineplus.gov/genetics/gene/dsp - Genetics
  9. TINF2 gene 
    ... report and review of the literature. Int J Dent Hyg. 2010 Feb;8(1):68-74. doi: 10.1111/j.1601-5037. ...
    https://medlineplus.gov/genetics/gene/tinf2 - Genetics
  10. Dyskeratosis congenita 
    ... report and review of the literature. Int J Dent Hyg. 2010 Feb;8(1):68-74. doi: 10.1111/j.1601-5037. ...
    https://medlineplus.gov/genetics/condition/dyskeratosis-congenita - Genetics
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