 Ectodermal Dysplasia
"Ectodermal Dysplasia" 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.
A group of hereditary disorders involving tissues and structures derived from the embryonic ectoderm. They are characterized by the presence of abnormalities at birth and involvement of both the epidermis and skin appendages. They are generally nonprogressive and diffuse. Various forms exist, including anhidrotic and hidrotic dysplasias, FOCAL DERMAL HYPOPLASIA, and aplasia cutis congenita.
| Descriptor ID |
D004476
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| MeSH Number(s) |
C16.131.077.350 C16.131.831.350 C16.320.850.250 C17.800.804.350 C17.800.827.250
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| Concept/Terms |
Ectodermal Dysplasia- Ectodermal Dysplasia
- Dysplasia, Ectodermal
- Dysplasias, Ectodermal
- Ectodermal Dysplasias
- Defect, Congenital Ectodermal
- Ectodermal Defect, Congenital
- Congenital Ectodermal Defect
- Congenital Ectodermal Defects
- Defects, Congenital Ectodermal
- Ectodermal Defects, Congenital
Hidrotic Ectodermal Dysplasia- Hidrotic Ectodermal Dysplasia
- Dysplasia, Hidrotic Ectodermal
- Dysplasias, Hidrotic Ectodermal
- Hidrotic Ectodermal Dysplasias
- Clouston Syndrome
- Syndrome, Clouston
- Hydrotic Ectodermal Dysplasia
- Dysplasia, Hydrotic Ectodermal
- Dysplasias, Hydrotic Ectodermal
- Ectodermal Dysplasia, Hydrotic
- Ectodermal Dysplasias, Hydrotic
- Hydrotic Ectodermal Dysplasias
- Ectodermal Dysplasia, Hidrotic
- Ectodermal Dysplasia, Hidrotic, Autosomal Dominant
- Clouston Hidrotic Ectodermal Dysplasia
- Clouston's Syndrome
- Cloustons Syndrome
- Syndrome, Clouston's
Anhidrotic Ectodermal Dysplasia- Anhidrotic Ectodermal Dysplasia
- Anhidrotic Ectodermal Dysplasias
- Dysplasia, Anhidrotic Ectodermal
- Dysplasias, Anhidrotic Ectodermal
- Ectodermal Dysplasias, Anhidrotic
- Ectodermal Dysplasia Anhidrotic
- Anhidrotic, Ectodermal Dysplasia
- Anhidrotics, Ectodermal Dysplasia
- Dysplasia Anhidrotic, Ectodermal
- Dysplasia Anhidrotics, Ectodermal
- Ectodermal Dysplasia, Anhydrotic
- Anhydrotic Ectodermal Dysplasia
- Anhydrotic Ectodermal Dysplasias
- Dysplasia, Anhydrotic Ectodermal
- Dysplasias, Anhydrotic Ectodermal
- Ectodermal Dysplasias, Anhydrotic
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Below are MeSH descriptors whose meaning is more general than "Ectodermal Dysplasia".
Below are MeSH descriptors whose meaning is more specific than "Ectodermal Dysplasia".
This graph shows the total number of publications written about "Ectodermal Dysplasia" by people in UAMS Profiles by year, and whether "Ectodermal Dysplasia" 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 |
|---|
| 2021 | 1 | 0 | 1 | | 2017 | 1 | 0 | 1 | | 2015 | 1 | 0 | 1 | | 2012 | 1 | 0 | 1 | | 1996 | 1 | 0 | 1 | | 1994 | 0 | 1 | 1 | | 1990 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Ectodermal Dysplasia" by people in Profiles over the past ten years.
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Weaver KN, Care M, Wakefield E, Zarate YA, Skoch J, Gripp KW, Prada CE. Craniosynostosis is a feature of Costello syndrome. Am J Med Genet A. 2022 04; 188(4):1280-1286.
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Hassed S, Li S, Mulvihill J, Aston C, Palmer S. Adams-Oliver syndrome review of the literature: Refining the diagnostic phenotype. Am J Med Genet A. 2017 Mar; 173(3):790-800.
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Lam H, Dare S, Nguyen T, Austin T. Anesthesia for a pediatric patient with cardiofaciocutaneous syndrome. A A Case Rep. 2015 Apr 01; 4(7):95-6.
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