 Hypopigmentation
"Hypopigmentation" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A condition caused by a deficiency or a loss of melanin pigmentation in the epidermis, also known as hypomelanosis. Hypopigmentation can be localized or generalized, and may result from genetic defects, trauma, inflammation, or infections.
| Descriptor ID |
D017496
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| MeSH Number(s) |
C17.800.621.440
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Hypopigmentation".
Below are MeSH descriptors whose meaning is more specific than "Hypopigmentation".
This graph shows the total number of publications written about "Hypopigmentation" by people in this website by year, and whether "Hypopigmentation" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2006 | 0 | 1 | 1 | | 2014 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hypopigmentation" by people in Profiles.
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Mulligan KM, O'Connell KA, Coleman MS, da Silva A, Reddy M, Kim L, Bazzi N, Afrin A, Dellavalle RP. Current landscape of clinical trials for vitiligo: improving outcome standardization and trial diversity. Clin Exp Dermatol. 2023 07 07; 48(7):795-797.
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Eby JM, Kang HK, Klarquist J, Chatterjee S, Mosenson JA, Nishimura MI, Garrett-Mayer E, Longley BJ, Engelhard VH, Mehrotra S, Le Poole IC. Immune responses in a mouse model of vitiligo with spontaneous epidermal de- and repigmentation. Pigment Cell Melanoma Res. 2014 Nov; 27(6):1075-85.
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High WA, Pandya AG. Pilot trial of 1% pimecrolimus cream in the treatment of seborrheic dermatitis in African American adults with associated hypopigmentation. J Am Acad Dermatol. 2006 Jun; 54(6):1083-8.
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Spritz RA, Bailin T, Nicholls RD, Lee ST, Park SK, Mascari MJ, Butler MG. Hypopigmentation in the Prader-Willi syndrome correlates with P gene deletion but not with haplotype of the hemizygous P allele. Am J Med Genet. 1997 Jul 11; 71(1):57-62.
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Sviderskaya EV, Bennett DC, Ho L, Bailin T, Lee ST, Spritz RA. Complementation of hypopigmentation in p-mutant (pink-eyed dilution) mouse melanocytes by normal human P cDNA, and defective complementation by OCA2 mutant sequences. J Invest Dermatol. 1997 Jan; 108(1):30-4.
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