"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
|
| Concept/Terms |
Ectodermal Dysplasia- Ectodermal Dysplasia
- Dysplasia, Ectodermal
- Dysplasias, Ectodermal
- Ectodermal Dysplasias
- Ectodermal Defect, Congenital
- Congenital Ectodermal Defect
- Congenital Ectodermal Defects
- Defects, Congenital Ectodermal
- Ectodermal Defects, Congenital
- Defect, Congenital Ectodermal
Hidrotic Ectodermal Dysplasia- Hidrotic Ectodermal Dysplasia
- Dysplasia, Hidrotic Ectodermal
- Dysplasias, Hidrotic Ectodermal
- Hidrotic Ectodermal Dysplasias
- Hydrotic Ectodermal Dysplasia
- Dysplasia, Hydrotic Ectodermal
- Dysplasias, Hydrotic Ectodermal
- Ectodermal Dysplasia, Hydrotic
- Ectodermal Dysplasias, Hydrotic
- Hydrotic Ectodermal Dysplasias
- Ectodermal Dysplasia, Hidrotic
- Clouston Hidrotic Ectodermal Dysplasia
- Hidrotic Ectodermal Dysplasia, Autosomal Dominant
- Clouston Syndrome
- Syndrome, Clouston
- Ectodermal Dysplasia 2, Hidrotic
- Autosomal Dominant Hidrotic Ectodermal Dysplasia
- Clouston's Hidrotic Ectodermal Dysplasia
- Clouston's Syndrome
- Cloustons Syndrome
- Syndrome, Clouston's
- Ectodermal Dysplasia, Hidrotic, Autosomal Dominant
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
|
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 |
|---|
| 1997 | 1 | 0 | 1 |
| 1998 | 1 | 0 | 1 |
| 1999 | 3 | 0 | 3 |
| 2001 | 3 | 0 | 3 |
| 2005 | 3 | 0 | 3 |
| 2009 | 3 | 0 | 3 |
| 2010 | 1 | 0 | 1 |
| 2012 | 2 | 0 | 2 |
| 2013 | 2 | 0 | 2 |
| 2014 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2017 | 2 | 0 | 2 |
| 2020 | 0 | 1 | 1 |
| 2021 | 2 | 0 | 2 |
| 2023 | 1 | 0 | 1 |
| 2024 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Ectodermal Dysplasia" by people in Profiles.
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Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies. Hum Genet. 2024 Mar; 143(3):279-291.
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The 8th International RASopathies Symposium: Expanding research and care practice through global collaboration and advocacy. Am J Med Genet A. 2024 04; 194(4):e63477.
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Naked (N) mutant mice carry a nonsense mutation in the homeobox of Hoxc13. Exp Dermatol. 2022 03; 31(3):330-340.
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Multidisciplinary management of a previously unreported presentation of severe aplasia cutis congenita. Pediatr Dermatol. 2021 Mar; 38(2):472-476.
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UBR7 functions with UBR5 in the Notch signaling pathway and is involved in a neurodevelopmental syndrome with epilepsy, ptosis, and hypothyroidism. Am J Hum Genet. 2021 01 07; 108(1):134-147.
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RASopathies: A significant cause of polyhydramnios? Prenat Diagn. 2021 02; 41(3):362-367.
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A Human Stem Cell-Based System to Study?the?Role of TP63 Mutations in Ectodermal Dysplasias. J Invest Dermatol. 2018 07; 138(7):1662-1665.
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Orthotopic liver transplantation for Sensenbrenner syndrome. Pediatr Transplant. 2018 02; 22(1).
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Adams-Oliver Syndrome Type 2 in Association with Compound Heterozygous DOCK6 Mutations. Pediatr Dermatol. 2017 Sep; 34(5):e249-e253.
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Visual Diagnosis: A Baby with a Scalp Lesion, Rash, and Left-Foot Deformity. Pediatr Rev. 2017 Jun; 38(6):e20-e23.