Condition: Congenital Aniridia · Sponsor: Assistance Publique - Hôpitaux de Paris
Congenital aniridia is a pan-ocular genetic disease characterized by a partial or complete absence of the iris, hence its name. The prevalence ranges from 1 / 40,000 to 1 / 96,000 births, but it may be underestimated. This condition combines several types of eye damage and could associate systemic manifestations, with a variable phenotype and genotype. This study aims to identify eye and systemic manifestations in congenital aniridia and to determine the patients' knowledge of their own disease through a survey prepared by ophthalmologists from the Ophthalmology Department of Necker-Enfants Malades Hospital, reference center in France for this pathology. The patient fills it out only once.
This description comes directly from the study's public registry record.
Alejandra Daruich, MD, PhD · 1 44 38 19 69 · alejandra.daruich-matet@aphp.fr
Hélène Morel · 1 71 19 63 46 · helene.morel@aphp.fr
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| Hôpital Necker-Enfants Malades | Paris, France | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05390801