Albinism, Ocular Clinical Trial
Official title:
Genetic Determinant of Foveolar Hypoplasia in Parents of Albinos Children
Fovea plana could be the phenoyipic translation of a genetic anomaly in one of the genes identified in albinisme
n/a
Status | Clinical Trial | Phase | |
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Recruiting |
NCT04495218 -
NGS Panel of Incomplete Forms of Ocular Albinism
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Not yet recruiting |
NCT06345976 -
Functional Impairment in Albinism
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Completed |
NCT00001153 -
Visual Function and Ocular Pigmentation in Albinism
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N/A |