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Results 21 - 22 of 22 for Congenital blindness
  1. Knobloch syndrome 
    ... and macula, people with Knobloch syndrome often develop blindness in one or both eyes.Another characteristic feature ... Joffe L, Spark RP, Smith BL, Hoyme HE. Congenital scalp defects and vitreoretinal degeneration: redefining the Knobloch ...
    https://medlineplus.gov/genetics/condition/knobloch-syndrome - Genetics
  2. WFS1 gene 
    ... cells along the optic nerve eventually leads to blindness in affected individuals. The death of cells in ... Vialettes B. Autosomal dominant transmission of diabetes and congenital hearing impairment secondary to a missense mutation in ...
    https://medlineplus.gov/genetics/gene/wfs1 - Genetics
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