"Pigmentation Disorders" 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.
Diseases affecting PIGMENTATION, including SKIN PIGMENTATION.
Descriptor ID |
D010859
|
MeSH Number(s) |
C17.800.621 C23.550.755
|
Concept/Terms |
Pigmentation Disorders- Pigmentation Disorders
- Disorder, Pigmentation
- Disorders, Pigmentation
- Pigmentation Disorder
Schamberg Disease- Schamberg Disease
- Disease, Schamberg
- Schamberg's Disease
- Disease, Schamberg's
- Schambergs Disease
Ito Syndrome- Ito Syndrome
- Syndrome, Ito
- Incontinentia Pigmenti Achromians
|
Below are MeSH descriptors whose meaning is more general than "Pigmentation Disorders".
Below are MeSH descriptors whose meaning is more specific than "Pigmentation Disorders".
This graph shows the total number of publications written about "Pigmentation Disorders" by people in this website by year, and whether "Pigmentation Disorders" 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 |
---|
2007 | 1 | 0 | 1 |
2011 | 1 | 0 | 1 |
2018 | 0 | 1 | 1 |
2020 | 1 | 0 | 1 |
2023 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Pigmentation Disorders" by people in Profiles.
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Pagani K, Plumptre I, Amin S, Lal K, Wiss K, Belazarian L. Low rates of neurological abnormalities in patients with pigmentary mosaicism: A retrospective cohort study from a tertiary dermatology center. Pediatr Dermatol. 2023 May-Jun; 40(3):446-451.
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Egbeto IA, Garelli CJ, Piedra-Mora C, Wong NB, David CN, Robinson NA, Richmond JM. Case Series: Gene Expression Analysis in Canine Vogt-Koyanagi-Harada/Uveodermatologic Syndrome and Vitiligo Reveals Conserved Immunopathogenesis Pathways Between Dog and Human Autoimmune Pigmentary Disorders. Front Immunol. 2020; 11:590558.
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Fukuda K, Harris JE. Vitiligo-like depigmentation in patients receiving programmed cell death-1 inhibitor reflects active vitiligo. J Am Acad Dermatol. 2018 01; 78(1):e15-e16.
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Gray C, Greenlaw SM, Alavian C, Wiss K. Epidermolysis bullosa simplex with mottled pigmentation: a novel KRT14 mutation. J Drugs Dermatol. 2011 Aug; 10(8):926-7.
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Aaron RS, Zacharias I, Mannion S, Gordon FD. Rare cutaneous manifestation of hyperbilirubinemia. Arch Dermatol. 2010 Feb; 146(2):209-10.
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Lee H, Carlin AM, Ormsby AH, Lee MW. Brown bowel syndrome secondary to jejunoileal bypass: the first case report. Obes Surg. 2009 Aug; 19(8):1176-9.
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Jellinek N. Nail matrix biopsy of longitudinal melanonychia: diagnostic algorithm including the matrix shave biopsy. J Am Acad Dermatol. 2007 May; 56(5):803-10.
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Johnson MD, Jacobs AH. Congenital smooth muscle hamartoma. A report of six cases and a review of the literature. Arch Dermatol. 1989 Jun; 125(6):820-2.