Profiles RNS Covid Authors

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.

MeSH information

Definition

Details

More General Concepts

Related Concepts

More Specific Concepts

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
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 Aplasia Cutis Congenita Aplasia Cutis Congenita Aplasia Cutis Congenita, Nonsyndromic 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".

Diseases [C]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Abnormalities, Multiple [C16.131.077]
Ectodermal Dysplasia [C16.131.077.350]
Skin Abnormalities [C16.131.831]
Ectodermal Dysplasia [C16.131.831.350]
Genetic Diseases, Inborn [C16.320]
Skin Diseases, Genetic [C16.320.850]
Ectodermal Dysplasia [C16.320.850.250]
Skin and Connective Tissue Diseases [C17]
Skin Diseases [C17.800]
Skin Abnormalities [C17.800.804]
Ectodermal Dysplasia [C17.800.804.350]
Skin Diseases, Genetic [C17.800.827]
Ectodermal Dysplasia [C17.800.827.250]

Below are MeSH descriptors whose meaning is related to "Ectodermal Dysplasia".

Below are MeSH descriptors whose meaning is more specific than "Ectodermal Dysplasia".

Publications

Timeline | Most Recent

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.

Bar chart showing 15 publications over 4 distinct years, with a maximum of 8 publications in 2017

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

Year	Major Topic	Minor Topic	Total
2017	8	0	8
2018	3	1	4
2019	2	0	2
2021	0	1	1

Below are the most recent publications written about "Ectodermal Dysplasia" by people in Profiles.

Management of COVID-19 pneumonia in a child with NEMO deficiency. Immunol Res. 2021 08; 69(4):391-393.

View in: PubMed
"Health status of children with chronic liver disease during the SARS-CoV-2 outbreak: results from a multicentre study". Clin Res Hepatol Gastroenterol. 2021 Mar; 45(2):101610.

View in: PubMed
COVID-19 and ectodermal dysplasias. Recommendations are necessary. Dermatol Ther. 2020 09; 33(5):e13702.

View in: PubMed
Using of modified rapid palate expander with miniscrews in a patient affected by ectodermic dysplasia. Clin Ter. 2019 May-Jun; 170(3):e168-e173.

View in: PubMed
Anatomical analysis of zygomatic bone in ectodermal dysplasia patients with oligodontia. Clin Implant Dent Relat Res. 2019 Apr; 21(2):310-316.

View in: PubMed
Trichoscopy in Hair Shaft Disorders. Dermatol Clin. 2018 Oct; 36(4):421-430.

View in: PubMed
Oral Mucosa-Derived Induced Pluripotent Stem Cells from Patients with Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome. Cell Reprogram. 2018 08; 20(4):215-224.

View in: PubMed
Induced pluripotent stem cells line (UNIPDi003-A) from a patient affected by EEC syndrome carrying the R279H mutation in TP63 gene. Stem Cell Res. 2018 04; 28:141-144.

View in: PubMed
Integrating Functional Analysis in the Next-Generation Sequencing Diagnostic Pipeline of RASopathies. Sci Rep. 2018 02 05; 8(1):2421.

View in: PubMed
WNT10A gene is the second molecular candidate in a cohort of young Italian subjects with ectodermal derivative impairment (EDI). Clin Genet. 2018 03; 93(3):693-698.

View in: PubMed

People

D'Antiga, Lorenzo

Explore

Top Journals

COVID A

UTHORS

Online profiles of coronavirus experts

Ectodermal Dysplasia