Add to ORKGAlbinism refers to a group of genetically - determined disorders characterized by deficient melanin production and congenital hypopigmentation. Recognized ocular manifestations of albinism include nystagmus, iris transillumination, and macular hypoplasia. Abnormalities of the optic disc have been described but have never been fully characterized
Purpose: To describe the phenotypic spectrum of a large cohort of albino patients, to investigate th...
Albinism is a group of rare inherited disorders arising from impairment of melanin biosynthesis. The...
Congenital optic disc pigmentation is a condition in which melanin deposition anterior to or within ...
Albinism is a hereditary condition characterized by hypopigmentation in the skin, eye and hair due t...
Albinism refers to a group of genetic abnormalities that are associated with profound defects throug...
Albinism is an uncommon genetic condition characterised by hypopigmentation of the hair, skin and ey...
Purpose: Albinism is a rare genetic disorder of melanin production, which can affect only eyes or si...
PURPOSE. The purpose of this study was to further expand the mutational spectrum of the Foveal Hypop...
Albinism is a group of hereditary pathologies characterized by a violation or complete absence of sk...
Purpose: The purpose of this thesis is to provide a comprehensive literature review about albinism a...
PURPOSE: To describe the phenotypic spectrum of a large cohort of albino patients, to investigate th...
Albinism describes a heterogeneous group of genetically determined disorders characterized by disrup...
Albinism is a pigment disorder affecting eye, skin and/or hair. Patients usually have decreased mela...
AbstractAlbinism, an inherited disorder of melanin biosynthesis, disrupts normal retinal development...
Albinism is a worldwide genetic disorder caused by mutations in at least 20 genes, identified to dat...
Purpose: To describe the phenotypic spectrum of a large cohort of albino patients, to investigate th...
Albinism is a group of rare inherited disorders arising from impairment of melanin biosynthesis. The...
Congenital optic disc pigmentation is a condition in which melanin deposition anterior to or within ...
Albinism is a hereditary condition characterized by hypopigmentation in the skin, eye and hair due t...
Albinism refers to a group of genetic abnormalities that are associated with profound defects throug...
Albinism is an uncommon genetic condition characterised by hypopigmentation of the hair, skin and ey...
Purpose: Albinism is a rare genetic disorder of melanin production, which can affect only eyes or si...
PURPOSE. The purpose of this study was to further expand the mutational spectrum of the Foveal Hypop...
Albinism is a group of hereditary pathologies characterized by a violation or complete absence of sk...
Purpose: The purpose of this thesis is to provide a comprehensive literature review about albinism a...
PURPOSE: To describe the phenotypic spectrum of a large cohort of albino patients, to investigate th...
Albinism describes a heterogeneous group of genetically determined disorders characterized by disrup...
Albinism is a pigment disorder affecting eye, skin and/or hair. Patients usually have decreased mela...
AbstractAlbinism, an inherited disorder of melanin biosynthesis, disrupts normal retinal development...
Albinism is a worldwide genetic disorder caused by mutations in at least 20 genes, identified to dat...
Purpose: To describe the phenotypic spectrum of a large cohort of albino patients, to investigate th...
Albinism is a group of rare inherited disorders arising from impairment of melanin biosynthesis. The...
Congenital optic disc pigmentation is a condition in which melanin deposition anterior to or within ...