
Albinism in humans - Wikipedia
Albinism is a congenital condition characterized in humans by the partial or complete absence of pigment in the skin, hair and eyes. Albinism is associated with a number of vision defects, …
Albinism - Symptoms and causes - Mayo Clinic
Dec 13, 2023 · Symptoms of albinism involve skin, hair and eye color, as well as vision. The easiest form of albinism to see results in white hair and very light-colored skin compared with …
Albinism: Types, Symptoms & Causes - Cleveland Clinic
Aug 12, 2024 · What does albino mean? The word “albino” comes from the Latin word “albus,” which means white. You might hear someone use “albino” to refer to a person with albinism. …
Albinism: Causes, Types, Pictures, Symptoms, and More
Apr 19, 2023 · Albinism is a rare genetic condition that causes the lack of pigment in skin, hair, and eyes, sometimes accompanied by visual impairment. Different types of albinism are …
Albinism: Symptoms, Causes, Types, Prevention, Risks and More
So far, doctors have identified seven different genetic issues that cause albinism in people with OCA.
What Causes Albinism and How It Affects Your Health
Nov 21, 2025 · Albinism is a genetic disease that causes a lack of melanin, which results in pale skin and sensitivity to sunlight. Sunscreen and protective clothing can help protect your skin if …
Albinism: Symptoms, Causes, Diagnosis & Treatment - WebMD
Jul 17, 2025 · Different types of albinism stem from defects in different enzymes and proteins in your DNA.
ALBINO Definition & Meaning - Merriam-Webster
The meaning of ALBINO is an organism exhibiting deficient pigmentation; especially : a human being who is congenitally deficient in pigment and usually has a milky or translucent skin, …
About Albinism & Hypopigmentation
Albinism is an inherited genetic condition that reduces the amount of melanin pigment formed in the skin, hair and/or eyes. Albinism occurs in all racial and ethnic groups throughout the world. …
About albinism. Beyond Race, Ethnicity and Gender - OHCHR
Albinism is a rare, non-contagious, genetically inherited condition which occurs worldwide regardless of ethnicity or gender.