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Results 1 - 4 of 4 for Knobloch syndrome
  1. Knobloch syndrome 
    Knobloch syndrome is a rare condition characterized by severe vision problems and a skull defect.A characteristic feature of Knobloch syndrome is extreme nearsightedness (high myopia). In addition, several ...
    https://medlineplus.gov/genetics/condition/knobloch-syndrome - Genetics
  2. COL18A1 gene 
    ... COL18A1 gene have been identified in people with Knobloch syndrome, a condition characterized by severe vision problems and ... protein likely causes the signs and symptoms of Knobloch syndrome. It is unclear whether endostatin is involved in ...
    https://medlineplus.gov/genetics/gene/col18a1 - Genetics
  3. Nearsightedness 
    ... pigmentosa, cone-rod dystrophy, deafness and myopia syndrome, Knobloch syndrome, and Cohen syndrome. Because common myopia is a ...
    https://medlineplus.gov/genetics/condition/nearsightedness - Genetics
  4. Retinal Disorders (National Library of Medicine)  
    The retina is a layer of tissue in the back of your eye that senses light and sends images to your brain. In the center of this nerve tissue is the macula. ...
    https://medlineplus.gov/retinaldisorders.html - Health Topics