Skin Abnormalities

"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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

Congenital structural abnormalities of the skin.

Descriptor ID	D012868
MeSH Number(s)	C16.131.831 C17.800.804
Concept/Terms	Skin Abnormalities Skin Abnormalities Abnormalities, Skin Abnormality, Skin Skin Abnormality

Below are MeSH descriptors whose meaning is more general than "Skin Abnormalities".

Diseases [C]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Skin Abnormalities [C16.131.831]
Skin and Connective Tissue Diseases [C17]
Skin Diseases [C17.800]
Skin Abnormalities [C17.800.804]

Below are MeSH descriptors whose meaning is related to "Skin Abnormalities".

Below are MeSH descriptors whose meaning is more specific than "Skin Abnormalities".

publications

Timeline | Most Recent

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.

Bar chart showing 7 publications over 7 distinct years, with a maximum of 1 publications in 1998 and 2004 and 2007 and 2014 and 2017 and 2020 and 2023

To see the data from this visualization as text, click here.

Year	Major Topic	Total
1998	1	1
2004	1	1
2007	1	1
2014	1	1
2017	1	1
2020	1	1
2023	1	1

Below are the most recent publications written about "Skin Abnormalities" by people in Profiles.

McElroy A, Gray-Edwards H, Coghill LM, Lyons LA. Precision medicine using whole genome sequencing in a cat identifies a novel COL5A1 variant for classical Ehlers-Danlos syndrome. J Vet Intern Med. 2023 Sep-Oct; 37(5):1716-1724.

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Leonard N, Droms R, Lal K, Amano S, Wiss K. Pink, waxy papule on the penile shaft. Pediatr Dermatol. 2020 Nov; 37(6):1151-1152.

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Sundberg JP, Dadras SS, Silva KA, Kennedy VE, Garland G, Murray SA, Sundberg BA, Schofield PN, Pratt CH. Systematic screening for skin, hair, and nail abnormalities in a large-scale knockout mouse program. PLoS One. 2017; 12(7):e0180682.

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Dean SJ, Holden KR, Dwivedi A, Dupont BR, Lyons MJ. Acquired microcephaly in blepharophimosis-ptosis-epicanthus inversus syndrome because of an interstitial 3q22.3q23 deletion. Pediatr Neurol. 2014 Jun; 50(6):636-9.

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Salmon Hillbertz NH, Isaksson M, Karlsson EK, Hellm?n E, Pielberg GR, Savolainen P, Wade CM, von Euler H, Gustafson U, Hedhammar A, Nilsson M, Lindblad-Toh K, Andersson L, Andersson G. Duplication of FGF3, FGF4, FGF19 and ORAOV1 causes hair ridge and predisposition to dermoid sinus in Ridgeback dogs. Nat Genet. 2007 Nov; 39(11):1318-20.

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Weiss G, Confino Y, Shemer A, Trau H. Cutaneous manifestations in the cardiofaciocutaneous syndrome, a variant of the classical Noonan syndrome. Report of a case and review of the literature. J Eur Acad Dermatol Venereol. 2004 May; 18(3):324-7.

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Kobielak K, Pasolli HA, Alonso L, Polak L, Fuchs E. Defining BMP functions in the hair follicle by conditional ablation of BMP receptor IA. J Cell Biol. 2003 Nov 10; 163(3):609-23.

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Pelsue SC, Schweitzer PA, Schweitzer IB, Christianson SW, Gott B, Sundberg JP, Beamer WG, Shultz LD. Lymphadenopathy, elevated serum IgE levels, autoimmunity, and mast cell accumulation in flaky skin mutant mice. Eur J Immunol. 1998 Apr; 28(4):1379-88.

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Shultz LD. Pleiotropic mutations causing abnormalities in the murine immune system and the skin. Curr Probl Dermatol. 1987; 17:236-50.

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