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Updated: Aug 14, 2026
13:26
Measuring Connectivity in the Primary Visual Pathway in Human Albinism Using Diffusion Tensor Imaging and Tractography
Published on: August 11, 2016
[Aniridia in a family characterized by low penetration]
Journal De Genetique Humaine
|February 1, 1981
Abstract:
Familial aniridia is an hereditary condition with dominant transmission. The frequency of associated lesions appears to indicate that absence of the iris is only the primary sign of an anomaly of development of the entire eye, derivatives of the ectoderm being predominantly affected. The authors examined the presence of familial anridia through 4 generations, characterized by low penetration and cataract predominantly of the right eye.
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