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 | |
|---|---|---|---|
| Recruiting |
NCT04495218 -
NGS Panel of Incomplete Forms of Ocular Albinism
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| Not yet recruiting |
NCT06345976 -
Functional Impairment in Albinism
|
||
| Completed |
NCT00001153 -
Visual Function and Ocular Pigmentation in Albinism
|
N/A |