"Skin Abnormalities" 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.
Congenital structural abnormalities of the skin.
| Descriptor ID |
D012868
|
| MeSH Number(s) |
C16.131.831 C17.800.804
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Skin Abnormalities".
Below are MeSH descriptors whose meaning is more specific than "Skin Abnormalities".
This graph shows the total number of publications written about "Skin Abnormalities" by people in this website by year, and whether "Skin Abnormalities" 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 | 0 | 1 | 1 |
| 2017 | 2 | 0 | 2 |
| 2018 | 1 | 0 | 1 |
| 2019 | 0 | 1 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Skin Abnormalities" by people in Profiles.
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Congenital Hypopigmentary Disorders with Multiorgan Impairment: A Case Report and an Overview on Gray Hair Syndromes. Medicina (Kaunas). 2019 Mar 25; 55(3).
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Insights into Mutation Effect in Three Poikiloderma with Neutropenia Patients by Transcript Analysis and Disease Evolution of Reported Patients with the Same Pathogenic Variants. J Clin Immunol. 2018 05; 38(4):494-502.
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Identification of a novel FOXL2 mutation in a single family with both types of blepharophimosis--ptosis-epicanthus inversus syndrome. Mol Med Rep. 2017 Oct; 16(4):5529-5532.
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Image Gallery: PELVIS syndrome. Br J Dermatol. 2017 02; 176(2):e14.
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Birthmarks and transient skin lesions in newborns and their relationship to maternal factors: a preliminary report from northern Italy. Dermatology. 2007; 215(1):53-8.