Oculocutaneous albinism, type 1A
Oculocutaneous albinism, type 1A: Introduction
Oculocutaneous albinism, type 1A: A rare inherited disorder characterized by complete lack of pigmentation in the skin, eyes and hair. Type 1A involves a complete absence of tyrosinase which is needed for the production of melanin which gives the skin, hair and eyes their color. It is caused by mutations in the TYR gene.
More detailed information about the symptoms,
causes, and treatments of Oculocutaneous albinism, type 1A is available below.
Symptoms of Oculocutaneous albinism, type 1A
See full list of 9
symptoms of Oculocutaneous albinism, type 1A
Home Diagnostic Testing
Home medical testing related to Oculocutaneous albinism, type 1A:
- Vision & Eye Health: Home Testing:
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Wrongly Diagnosed with Oculocutaneous albinism, type 1A?
Oculocutaneous albinism, type 1A: Deaths
Read more about Deaths and Oculocutaneous albinism, type 1A.
Oculocutaneous albinism, type 1A: Complications
Review possible medical complications related to Oculocutaneous albinism, type 1A:
Causes of Oculocutaneous albinism, type 1A
Read more about causes of Oculocutaneous albinism, type 1A.
Disease Topics Related To Oculocutaneous albinism, type 1A
Research the causes of these diseases that are similar to, or related to, Oculocutaneous albinism, type 1A:
Oculocutaneous albinism, type 1A: Undiagnosed Conditions
Commonly undiagnosed diseases in related medical categories:
Misdiagnosis and Oculocutaneous albinism, type 1A
Psoriasis often undiagnosed cause of skin symptoms in children: Children who suffer
from the skin disorder called psoriasis can often go undiagnosed.
The...read more »
Read more about Misdiagnosis and Oculocutaneous albinism, type 1A
Oculocutaneous albinism, type 1A: Research Doctors & Specialists
Research related physicians and medical specialists:
Other doctor, physician and specialist research services:
Oculocutaneous albinism, type 1A: Animations
More Oculocutaneous albinism, type 1A animations & videos
Statistics for Oculocutaneous albinism, type 1A
Oculocutaneous albinism, type 1A: Broader Related Topics
Types of Oculocutaneous albinism, type 1A
User Interactive Forums
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Definitions of Oculocutaneous albinism, type 1A:
Oculocutaneous albinism, type 1A is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Oculocutaneous albinism, type 1A, or a subtype of Oculocutaneous albinism, type 1A,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Contents for Oculocutaneous albinism, type 1A:
- Oculocutaneous albinism, type 1A
- What is Oculocutaneous albinism, type 1A?
- Prevalence and Incidence of Oculocutaneous albinism, type 1A
- Videos related to Oculocutaneous albinism, type 1A
- Causes of Oculocutaneous albinism, type 1A
- Symptoms of Oculocutaneous albinism, type 1A
- Diagnostic Tests for Oculocutaneous albinism, type 1A
- Home Testing and Oculocutaneous albinism, type 1A
- Signs of Oculocutaneous albinism, type 1A
- Complications of Oculocutaneous albinism, type 1A
- Misdiagnosis of Oculocutaneous albinism, type 1A
- Undiagnosed Oculocutaneous albinism, type 1A
- Inheritance and Genetics of Oculocutaneous albinism, type 1A
- Contagious: Oculocutaneous albinism, type 1A
- Treatments for Oculocutaneous albinism, type 1A
- Doctors and Medical Specialists for Oculocutaneous albinism, type 1A
- Deaths from Oculocutaneous albinism, type 1A
- Statistics about Oculocutaneous albinism, type 1A
- Glossary for Oculocutaneous albinism, type 1A