 Skin Diseases, Genetic
"Skin Diseases, Genetic" 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 of the skin with a genetic component, usually the result of various inborn errors of metabolism.
| Descriptor ID |
D012873
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| MeSH Number(s) |
C16.320.850 C17.800.827
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| Concept/Terms |
Skin Diseases, Genetic- Skin Diseases, Genetic
- Genetic Skin Diseases
- Disease, Genetic Skin
- Diseases, Genetic Skin
- Genetic Skin Disease
- Skin Disease, Genetic
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Below are MeSH descriptors whose meaning is more general than "Skin Diseases, Genetic".
Below are MeSH descriptors whose meaning is more specific than "Skin Diseases, Genetic".
- Skin Diseases, Genetic
- Albinism
- Cutis Laxa
- Darier Disease
- Dermatitis, Atopic
- Dyskeratosis Congenita
- Ectodermal Dysplasia
- Ehlers-Danlos Syndrome
- Epidermolysis Bullosa
- Erythrokeratodermia Variabilis
- Hyalinosis, Systemic
- Ichthyosiform Erythroderma, Congenital
- Ichthyosis Bullosa of Siemens
- Ichthyosis Vulgaris
- Ichthyosis, X-Linked
- Incontinentia Pigmenti
- Keratoderma, Palmoplantar
- Leukokeratosis, Hereditary Mucosal
- Lipoid Proteinosis of Urbach and Wiethe
- Monilethrix
- Netherton Syndrome
- Pemphigus, Benign Familial
- Porokeratosis
- Porphyria, Erythropoietic
- Porphyrias, Hepatic
- Prolidase Deficiency
- Pseudoxanthoma Elasticum
- Rothmund-Thomson Syndrome
- Sjogren-Larsson Syndrome
- Trichothiodystrophy Syndromes
- Xeroderma Pigmentosum
This graph shows the total number of publications written about "Skin Diseases, Genetic" by people in UAMS Profiles by year, and whether "Skin Diseases, Genetic" 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 |
|---|
| 2023 | 2 | 0 | 2 | | 2018 | 1 | 0 | 1 | | 2017 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Skin Diseases, Genetic" by people in Profiles over the past ten years.
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Masson R, Ma E, Park S, Dagenet CB, Crew AB, Hughes M, Shi VY, Hsiao JL. Top cited articles in dissecting cellulitis of the scalp: A bibliometric analysis. Skin Res Technol. 2023 Nov; 29(11):e13509.
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Vijayan V, Sukumaran S. Erythema Marginatum. J Pediatr. 2023 07; 258:113330.
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Ly S, Guram M, Zoumberos N, Kincannon J, Evans MS. Annular erythema of infancy: A rare and challenging diagnosis. Pediatr Dermatol. 2023 Jul-Aug; 40(4):681-687.
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Beyens A, Albuisson J, Boel A, Al-Essa M, Al-Manea W, Bonnet D, Bostan O, Boute O, Busa T, Canham N, Cil E, Coucke PJ, Cousin MA, Dasouki M, De Backer J, De Paepe A, De Schepper S, De Silva D, Devriendt K, De Wandele I, Deyle DR, Dietz H, Dupuis-Girod S, Fontenot E, Fischer-Zirnsak B, Gezdirici A, Ghoumid J, Giuliano F, Di?z NB, Haider MZ, Hardin JS, Jeunemaitre X, Klee EW, Kornak U, Landecho MF, Legrand A, Loeys B, Lyonnet S, Michael H, Moceri P, Mohammed S, Mui?o-Mosquera L, Nampoothiri S, Pichler K, Prescott K, Rajeb A, Ramos-Arroyo M, Rossi M, Salih M, Seidahmed MZ, Schaefer E, Steichen-Gersdorf E, Temel S, Uysal F, Vanhomwegen M, Van Laer L, Van Maldergem L, Warner D, Willaert A, Collins TR, Taylor A, Davis EC, Zarate Y, Callewaert B. Arterial tortuosity syndrome: 40 new families and literature review. Genet Med. 2018 10; 20(10):1236-1245.
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Hardin JS, Zarate YA, Callewaert B, Phillips PH, Warner DB. Ophthalmic findings in patients with arterial tortuosity syndrome and carriers: A case series. Ophthalmic Genet. 2018 Jan-Feb; 39(1):29-34.
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