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Hypopigmentation of the fundus

Known as: Decreased retinal pigmentation, DEPIGMENTATION RETINAL, Retinal hypopigmentation 
Decreased amount of pigmentation of the retina. [HPO:probinson]
National Institutes of Health

Related topics

Related topics

12 relations
Absent corpus callosum cataract immunodeficiencyAcrocallosal SyndromeBRAIN SMALL VESSEL DISEASE WITH OR WITHOUT OCULAR ANOMALIESEye - Retina (MMHCC)

Broader (2)

Hypopigmentation disorderRetinal Diseases

Papers overview

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Highly Cited
2011
Highly Cited
2011
Screening of TYR, OCA2, GPR143, and MC1R in patients with congenital nystagmus, macular hypoplasia, and fundus hypopigmentation indicating albinism
Background A broad spectrum of pigmentation of the skin and hair is found among patients diagnosed with ocular albinism (OA) and… 
2007
2007
Basic research confirms coexistence of acquired Blaschkolinear Vitiligo and acrofacial Vitiligo
We report about a female patient with bilateral and unilateral blaschkolinear depigmentation on the extremities and coexistence… 
2006
2006
Ocular Findings in Gillespie-Like Syndrome: Association with a New PAX6 Mutation
Background: Gillespie syndrome is a rare variant form of aniridia, characterized by mental retardation, nonprogressive cerebellar… 
2005
2005
Periocular Vitiligo with Onset Around a Congenital Divided Nevus of the Eyelid
Abstract:  Leukoderma in association with congenital melanocytic nevi is a rare phenomenon; nevertheless several reports have… 
2004
2004
Efficacy of spectacles in persons with albinism.
2002
2002
Prolonged childhood Cushing's syndrome secondary to intralesional triamcinolone acetonide
Abstract Intralesional corticosteroids have been used in the treatment of hypertrophic keloid scars for over 40 years. The few… 
Highly Cited
1999
Highly Cited
1999
Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation.
1997
1997
Multiple congenital anomalies, brain hypomyelination, and ocular albinism in a female with dup(X) (pter-->q24::q21.32-->qter) and random X inactivation.
We report on an 18-month-old girl with multiple congenital anomalies (prominence of the metopic suture, fine hair, club foot… 
1991
1991
Variable expression of albinism within a single kindred.
1958
1958
Leukomelanoderma subsequent to the application of monobenzyl ether of hydroquinone; a vitiligoid reaction observed in Colombia and Venezuela.
The role of monobenzyl ether of hydroquinone as a cause of depigmentation has been known since the report of Oliver, Schwartz… 
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