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Results 1 - 5 of 5 for Wolfram syndrome 1
  1. Wolfram syndrome 
    Wolfram syndrome is a condition that affects many of the body's systems. The hallmark features of Wolfram syndrome are high blood sugar (glucose) levels resulting ...
    https://medlineplus.gov/genetics/condition/wolfram-syndrome - Genetics
  2. WFS1 gene 
    ... the WFS1 gene have been found to cause Wolfram syndrome. This condition is characterized by a lack of ... gene in each cell are necessary to cause Wolfram syndrome. Some variants delete or insert pieces of DNA ...
    https://medlineplus.gov/genetics/gene/wfs1 - Genetics
  3. CISD2 gene 
    ... the CISD2 gene has been found to cause Wolfram syndrome. This condition is characterized by a lack of ... after injury.The CISD2 gene mutation that causes Wolfram syndrome replaces the amino acid glutamic acid with the ...
    https://medlineplus.gov/genetics/gene/cisd2 - Genetics
  4. Nonsyndromic hearing loss 
    ... CDH23 and MYO7A, among others), Pendred syndrome (SLC26A4), Wolfram syndrome (WFS1), and Stickler syndrome (COL11A2). It is often ...
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss - Genetics
  5. Nearsightedness 
    ... syndrome, it follows the inheritance pattern of that syndrome, most commonly autosomal ... VJ, Cumberland P, Bertelsen G, Wolfram C, Buitendijk GH, Hofman A, van Duijn CM, ...
    https://medlineplus.gov/genetics/condition/nearsightedness - Genetics