"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 |
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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 |
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1994 | 1 | 0 | 1 |
1995 | 1 | 1 | 2 |
1996 | 1 | 0 | 1 |
1997 | 1 | 0 | 1 |
1998 | 1 | 1 | 2 |
2000 | 0 | 1 | 1 |
2001 | 1 | 0 | 1 |
2002 | 2 | 0 | 2 |
2005 | 1 | 0 | 1 |
2006 | 1 | 0 | 1 |
2012 | 0 | 1 | 1 |
2013 | 2 | 0 | 2 |
2014 | 2 | 0 | 2 |
2016 | 1 | 0 | 1 |
2018 | 1 | 0 | 1 |
2019 | 1 | 0 | 1 |
2020 | 0 | 1 | 1 |
2022 | 2 | 0 | 2 |
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Below are the most recent publications written about "Skin Abnormalities" by people in Profiles.
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Topical trametinib for epidermal and sebaceous nevi in a child with Schimmelpenning-Feuerstein-Mims syndrome. Pediatr Dermatol. 2024 May-Jun; 41(3):523-525.
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Generalized birthmarks with glaucoma and lower extremity overgrowth. Pediatr Dermatol. 2023 03; 40(2):373-375.
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Hyaluronidase for Skin Necrosis Induced by Amiodarone. Cutis. 2022 10; 110(4):E33-E35.
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Erythematous Papule on the Nasal Ala. Cutis. 2022 09; 110(3):138-144.
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In Reply: "A nodular growth within a congenital birthmark: Diagnosis of non-involuting hemangioma is questioned". Pediatr Dermatol. 2021 05; 38(3):733.
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A solitary pink papule in a 14-year-old boy. Pediatr Dermatol. 2021 05; 38(3):e22-e23.
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Eruptive papules isolated to the anterior neck of a young woman. Pediatr Dermatol. 2020 07; 37(4):738-739.
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A nodular growth within a congenital birthmark. Pediatr Dermatol. 2020 07; 37(4):727-729.
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Refinement of the clinical and mutational spectrum of UBE2A deficiency syndrome. Clin Genet. 2020 08; 98(2):172-178.
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Hamartomas and midline anomalies in association with infantile hemangiomas, PHACE, and LUMBAR syndromes. Pediatr Dermatol. 2020 Jan; 37(1):78-85.