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Ocular Albinism
Summary
59
relevant articles (0 outcomes,
3 trials/studies)
found for this Disease
Description:
Albinism affecting the eye in which pigment of the hair and skin is normal or only slightly diluted. The classic type is X-linked (Nettleship-Falls), but an autosomal recessive form also exists. Ocular abnormalities may include reduced pigmentation of the iris, nystagmus, photophobia, strabismus, and decreased visual acuity.
Also Known As:
Albinism, Ocular
Key Drugs and Agents for Ocular Albinism
Efficacy Chart >>
Drugs and Important Biological Agents (IBA) related to treatments:
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Monophenol Monooxygenase (Tyrosinase)
:
2 studies in 11 results
: IBA
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Melanins (Melanin)
:
1 study in 6 results
: IBA
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Steryl-Sulfatase (Steroid Sulfatase)
:
1 study in 5 results
: IBA
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Retinaldehyde (Retinal)
:
11 results
: IBA
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Membrane Glycoproteins (Membrane Glycoprotein)
:
6 results
: IBA
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DNA (Deoxyribonucleic Acid)
:
6 results
: IBA
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GTP-Binding Proteins (G-Protein)
:
3 results
: IBA
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Glycoproteins (Glycoprotein)
:
2 results
: IBA
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Genetic Markers (Genetic Marker)
:
2 results
: IBA
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Universal
:
2 results
: IBA
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Diseases Related to Ocular Albinism
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Oculocutaneous Albinism (Albinism, Yellow Mutant)
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Albinism
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Hypopigmentation (Hypomelanosis)
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Kallmann Syndrome (Kallmann's Syndrome)
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X-Linked Ichthyosis (Ichthyosis, X Linked)
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Key Therapies for Ocular Albinism
Efficacy Chart >>
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Electrodes (Electrode)
:
1 result
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