"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
|
| MeSH Number(s) |
C17.800.621.440
|
| 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 |
|---|
| 2002 | 0 | 1 | 1 |
| 2005 | 1 | 0 | 1 |
| 2011 | 1 | 0 | 1 |
| 2013 | 2 | 0 | 2 |
| 2015 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2020 | 0 | 1 | 1 |
| 2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hypopigmentation" by people in Profiles.
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Ralph D, Levine MA, Richard G, Morrow MM, Flynn EK, Uitto J, Li Q. Mutation update: Variants of the ENPP1 gene in pathologic calcification, hypophosphatemic rickets, and cutaneous hypopigmentation with punctate keratoderma. Hum Mutat. 2022 09; 43(9):1183-1200.
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O'Sullivan S, Ozoemena L, Liu L, McGrath JA, Mellerio JE, Martinez AE. PLACK syndrome: the penny dropped. Clin Exp Dermatol. 2020 Dec; 45(8):1091-1092.
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Wang K, Nassef Y, Sahu J, Hermes H, Schwartz LR. Facial involvement in progressive macular hypomelanosis. Cutis. 2018 Apr; 101(4):297-300.
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Cuell A, Bansal N, Cole T, Kaur MR, Lee J, Loffeld A, Moss C, O'Donnell M, Takeichi T, Thind CK, McGrath JA. Familial progressive hyper- and hypopigmentation and malignancy in two families with new mutations in KITLG. Clin Exp Dermatol. 2015 Dec; 40(8):860-4.
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Eytan O, Morice-Picard F, Sarig O, Ezzedine K, Isakov O, Li Q, Ishida-Yamamoto A, Shomron N, Goldsmith T, Fuchs-Telem D, Adir N, Uitto J, Orlow SJ, Taieb A, Sprecher E. Cole Disease Results from Mutations in ENPP1. Am J Hum Genet. 2013 Oct 03; 93(4):752-7.
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Shields CL, Nickerson SJ, Al-Dahmash S, Shields JA. Waardenburg syndrome: iris and choroidal hypopigmentation: findings on anterior and posterior segment imaging. JAMA Ophthalmol. 2013 Sep; 131(9):1167-73.
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Say EA, Shields CL, Bianciotto C, Shields JA. Perilymphatic subcutaneous fat atrophy and cutaneous depigmentation after periocular triamcinolone acetonide injection in a child. J AAPOS. 2011 Feb; 15(1):107-8.
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Ang G, Hyde PM, Lee JB. Unilateral congenital linear atrophoderma of the leg. Pediatr Dermatol. 2005 Jul-Aug; 22(4):350-4.
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Shahidi M, Blair NP, Mori M, Gieser J, Pulido JS. Retinal topography and thickness mapping in atrophic age related macular degeneration. Br J Ophthalmol. 2002 Jun; 86(6):623-6.