 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
- Ectodermal Dysplasia, Hidrotic, Autosomal Dominant
- Hydrotic Ectodermal Dysplasia
- Dysplasia, Hydrotic Ectodermal
- Dysplasias, Hydrotic Ectodermal
- Ectodermal Dysplasia, Hydrotic
- Ectodermal Dysplasias, Hydrotic
- Hydrotic Ectodermal Dysplasias
- Ectodermal Dysplasia 2, Hidrotic
- Autosomal Dominant Hidrotic Ectodermal Dysplasia
- Clouston's Syndrome
- Cloustons Syndrome
- Syndrome, Clouston's
- Hidrotic Ectodermal Dysplasia, Autosomal Dominant
- Clouston Hidrotic Ectodermal Dysplasia
- Clouston Syndrome
- Syndrome, Clouston
- Ectodermal Dysplasia, Hidrotic
- Clouston's Hidrotic Ectodermal Dysplasia
Anhidrotic Ectodermal Dysplasia- Anhidrotic Ectodermal Dysplasia
- Anhidrotic Ectodermal Dysplasias
- Dysplasia, Anhidrotic Ectodermal
- Dysplasias, Anhidrotic Ectodermal
- Ectodermal Dysplasia, Anhidrotic
- 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 this website 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 |
|---|
| 2002 | 1 | 0 | 1 | | 2011 | 0 | 2 | 2 | | 2012 | 2 | 0 | 2 |
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Below are the most recent publications written about "Ectodermal Dysplasia" by people in Profiles.
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Chan RK, Liu AS, Rogers GF. Aplasia cutis congenita of the trunk associated with fetus papyraceous. J Craniofac Surg. 2012 Jul; 23(4):995-7.
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Wei J, Xue Y, Wu L, Ma J, Yi X, Zhang J, Lu B, Li C, Shi D, Shi S, Feng X, Cai T. Analysis of large phenotypic variability of EEC and SHFM4 syndromes caused by K193E mutation of the TP63 gene. PLoS One. 2012; 7(5):e35337.
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Rosenberg JB, Butrus S, Bazemore MG. Ectrodactyly-ectodermal dysplasia-clefting syndrome causing blindness in a child. J AAPOS. 2011 Feb; 15(1):80-2.
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Sripathomsawat W, Tanpaiboon P, Heering J, Dötsch V, Hennekam RC, Kantaputra P. Phenotypic analysis of Arg227 mutations of TP63 with emphasis on dental phenotype and micturition difficulties in EEC syndrome. Am J Med Genet A. 2011 Jan; 155A(1):228-32.
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DiFazio MP, Levin S, Depper M. Ectodermal dysplasia and brain cystic changes: confirmation of a novel neurocutaneous syndrome. J Child Neurol. 2002 Jul; 17(7):475-8.
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