ocular albinism

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Functional Impairment in Albinism	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, albinism, eye disorder, hereditary disease, hereditary skin disorder, hypopigmentation of the skin, inborn disorder of amino acid metabolism, inborn errors of metabolism, metabolic disease, ocular albinism, skin disorder, skin pigmentation disorder	Recruiting	Not stated	2025-02-13		NCT06345976

Clinical trials