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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 ...
- ... 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 ...
- ... pigmentosa, cone-rod dystrophy, deafness and myopia syndrome, Knobloch syndrome, and Cohen syndrome. Because common myopia is a ...
