Including results for congenital achromatopsia
Search only for congenital achromia
Achromasia, also known as albinism, is a set of inherited disorders that cause scant or no production of melanin, a natural skin pigment. The type and amount of melanin an individual's body produces determines the color of their skin, hair, and eyes. Melanin also has a role in the development of the optic nerves.
Achromatopsia, also known as rod monochromacy, is a medical syndrome that exhibits symptoms relating to five conditions, most notably monochromacy.
Aug 30, 2017 · Albinism (also called achromia, achromasia, or achromatosis) is a congenital disorder characterized by the complete or partial absence of ...
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Albinism is a congenital condition characterized in humans by the partial or complete absence of pigment in the skin, hair and eyes.
achromia · 1. Absence of color; pallor. · 2. Achromatosis. · 3. Condition in which erythrocytes have large central pale areas; hypochromia.
a visual defect that is marked by total color blindness in which the colors of the spectrum are seen as tones of white, gray, and black.
Albinism, also known as achromia, achromasia, or achromatosis, is a congenital condition characterised by the partial or complete absence of pigment in the skin ...
Generalised reduction in melanin pigmentation at birth (congenital) may be racial in origin or due to albinism. ... There is no effective treatment for achromia ...
Oct 26, 2021 · It is a rare, non-contagious congenital genetic disorder. It also lasts for life and does not get worse over time. People with albinism often look pale.
Oct 29, 2020 · Congenital or acquired loss of skin pigment, e.g. in albinism, vitiligo, leukoderm.
