| Health / Medical Topics |
Oculocutaneous Albinism
An autosomal recessive inherited disorder caused by mutations of the OCA2, SLC45A2, TYR and TYRP1 genes. It is characterized by hypopigmentation of the skin, hair, and eyes, resulting in very fair skin, white colored hair, and reduced pigmentation in the iris and retina. Individuals may have vision disturbances and photophobia. (NCI Thesaurus)
YOU MAY ALSO LIKE
An X-linked inherited multisystem metabolic disorder caused by mutations in the OCRL1 gene. The main manifestations of this disorder result from involvement…
A dosing unit equal to the amount of active ingredient(s) in an ocular system.
A system that is placed in the eye, usually under the lower eyelid, from which the active and/or inert ingredient(s) diffuses through…
Subdiscipline of pathology with a focus on vision and the eye.
Filarial infection of the eyes transmitted from person to person by bites of Onchocerca volvulus-infected black flies. The microfilariae of Onchocerca are…
A rare cancer of melanocytes (cells that produce the pigment melanin) found in the eye. Also called intraocular melanoma.
