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Results 1 - 1 of 1 for Pendred syndrome
  1. SLC26A4 gene 
    ... mutations in the SLC26A4 gene in people with Pendred syndrome. This condition is characterized by enlargement of the ... symptoms overlap, it can be difficult to distinguish Pendred syndrome from nonsyndromic hearing loss (DFNB4, described above). Many ...
    https://medlineplus.gov/genetics/gene/slc26a4 - Genetics