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Oculocutaneous Albinism
(Albinism, Yellow Mutant)
Summary
261
relevant articles (1 outcomes,
9 trials/studies)
found for this Disease
Description:
Heterogeneous group of autosomal recessive disorders comprising at least four recognized types, all having in common varying degrees of hypopigmentation of the skin, hair, and eyes. The two most common are the tyrosinase-positive and tyrosinase-negative types.
Also Known As:
Albinism, Yellow Mutant; Albinism, Oculocutaneous; Albinism, Tyrosinase Negative; Albinism, Tyrosinase Positive; Tyrosinase-Negative Albinism Show All >>
Key Drugs and Agents for Oculocutaneous Albinism
Efficacy Chart >>
Drugs and Important Biological Agents (IBA) related to treatments:
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Monophenol Monooxygenase (Tyrosinase)
:
1 outcome 5 studies in 163 results
: IBA
-
Melanins (Melanin)
:
1 study in 47 results
: IBA
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Proteins (Proteins, Gene)
:
1 study in 8 results
: IBA
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Copper
:
1 study in 5 results
: IBA
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Type 1 Melanocortin Receptor
:
1 study in 3 results
: IBA
-
Calcium
:
1 study in 1 result
: IBA
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Ceroid
:
33 results
: IBA
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Triad
:
15 results
:
FDA 1
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Lipofuscin
:
11 results
: IBA
-
Retinaldehyde (Retinal)
:
8 results
: IBA
Show All >>
Diseases Related to Oculocutaneous Albinism
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Syndrome
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Menkes Kinky Hair Syndrome (Menkes Disease)
-
Neurofibromatoses (Neurofibromatosis)
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Exfoliative Dermatitis (Erythroderma)
-
Hermanski-Pudlak Syndrome (Hermansky-Pudlak Syndrome)
Show All >>
Key Therapies for Oculocutaneous Albinism
Efficacy Chart >>
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Transplants (Transplant)
:
1 result
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Intraocular Lens Implantation
:
1 result
-
Skin Transplantation (Skin Grafting)
:
1 result
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