Albinism, Ocular Clinical Trial
Official title:
Functional Impairment in Albinism
Albinism is a genetic and hereditary anomaly that affects pigmentation. This pathology is characterized by a deficit in melanin production. In humans, the clinical diagnosis of albinism is based on a number of factors, including : - In the integumentary region: fair skin tone, with white hair, eyelashes and eyebrows. - Ophthalmological: reduced visual acuity, photophobia, nystagmus, transilluminated blue irises, hypopigmentation of the retina at the back of the eye with fovea plana. As treatment options begin to emerge for certain albinism-induced anomalies (including, for example, the depigmentation that causes photophobia), it is desirable to understand what these patients' complaints are, and to gather their views on the emergence of treatments targeting just one of their complaints, namely glare.
n/a
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Recruiting |
NCT04495218 -
NGS Panel of Incomplete Forms of Ocular Albinism
|
||
| Completed |
NCT00001153 -
Visual Function and Ocular Pigmentation in Albinism
|
N/A | |
| Completed |
NCT03959605 -
Genetic Determinant of Foveolar Hypoplasia in Parents of Albinos Children
|