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.

MeSH information

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

Diseases of the skin with a genetic component, usually the result of various inborn errors of metabolism.

Descriptor ID	D012873
MeSH Number(s)	C16.320.850 C17.800.827
Concept/Terms	Skin Diseases, Genetic Skin Diseases, Genetic Genetic Skin Diseases Disease, Genetic Skin Diseases, Genetic Skin Genetic Skin Disease Skin Disease, Genetic

Below are MeSH descriptors whose meaning is more general than "Skin Diseases, Genetic".

Diseases [C]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Skin Diseases, Genetic [C16.320.850]
Skin and Connective Tissue Diseases [C17]
Skin Diseases [C17.800]
Skin Diseases, Genetic [C17.800.827]

Below are MeSH descriptors whose meaning is related to "Skin Diseases, Genetic".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Skin Diseases, Genetic" by people in this website by year, and whether "Skin Diseases, Genetic" was a major or minor topic of these publications.

Bar chart showing 8 publications over 5 distinct years, with a maximum of 2 publications in 2015 and 2018 and 2019

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

Year	Major Topic	Total
2014	1	1
2015	2	2
2016	1	1
2018	2	2
2019	2	2

Below are the most recent publications written about "Skin Diseases, Genetic" by people in Profiles.

Lewis DJ, Wu JH, Boyd M, Duvic M, Feldman SR. Cutaneous manifestations of genodermatoses and primary immunodeficiency. Dermatol Online J. 2019 Jun 15; 25(6).

View in: PubMed
Smithee A, Garcia A, Tschen J, Schmidt J. Primary Localized Cutaneous Nodular Amyloidosis in the Absence of Systemic Disease. Skinmed. 2019; 17(2):131-133.

View in: PubMed
Shamim MM, Weissman HM, Al-Mohtaseb ZN. Treatment of Ligneous Conjunctivitis Using Topical Plasminogen Therapy in an 8-Week-Old Female Infant. J Pediatr Ophthalmol Strabismus. 2018 Aug 29; 55:e30-e32.

View in: PubMed
Russo ML, Sukhavasi N, Mathur V, Morris SA. Obstetric Management of Loeys-Dietz Syndrome. Obstet Gynecol. 2018 06; 131(6):1080-1084.

View in: PubMed
Shah K, Mehmood S, Jan A, Abbe I, Hussain Ali R, Khan A, Chishti MS, Lee K, Ahmad F, Ansar M, Shahzad S, Nickerson DA, Bamshad MJ, Coucke PJ, Santos-Cortez RLP, Spritz RA, Leal SM, Ahmad W. Sequence variants in nine different genes underlying rare skin disorders in 10 consanguineous families. Int J Dermatol. 2017 Dec; 56(12):1406-1413.

View in: PubMed
Plaza JA, Toussaint S, Prieto VG, Mercadillo P, Diez de Medina JC, Lourenco S, Batdorf B, Sangueza M. Actinic Prurigo Cheilitis: A Clinicopathologic Review of 75 Cases. Am J Dermatopathol. 2016 Jun; 38(6):418-22.

View in: PubMed
Morris SA. Arterial tortuosity in genetic arteriopathies. Curr Opin Cardiol. 2015 Nov; 30(6):587-93.

View in: PubMed
Ogunmakin K, Vangipuram R, Sturgeon A, Shimizu I. A 7-year-old with indurated skin and unilateral progressive joint immobility: A case of stiff skin syndrome. Dermatol Online J. 2015 Sep 17; 21(9).

View in: PubMed
Reinstein E, Morris SA, Rimoin DL, Robertson SP, Lacro RV. Arterial tortuosity in patients with Filamin A- associated vascular aneurysms. Am J Med Genet A. 2014 Nov; 164A(11):2961-3.

View in: PubMed