Results 61 to 70 of about 71,788 (137)

[Tooth disorders in ectodermal dysplasias]

open access: yes, 2003
Recently, the molecular bases of the most frequent ectodermal dysplasias have been identified; they involve genes responsible for the epithelial morphogenesis, and the regulation of cell survival and proliferation.
G. Rapelli   +2 more
core  

Connexin30 mutations responsible for hidrotic ectodermal dysplasia cause abnormal hemichannel activity

open access: yes, 2004
Clouston syndrome or hidrotic ectodermal dysplasia (HED) is a rare dominant genodermatosis characterized by palmoplantar hyperkeratosis, generalized alopecia and nail defects.
Meda, P   +7 more
core   +1 more source

Ellis-van Creveld with an Unusual Dental Anomaly: A Case Report

open access: yesIranian Journal of Medical Sciences, 2017
The Ellis-van Creveld (EVC) syndrome is a chondroectodermal dysplasia and is characterized by the cardinal features of disproportionate short stature, polydactyly, hidrotic ectodermal dysplasia, and congenital heart malformations, along with other ...
Suzanne Tanya Nethan   +2 more
doaj  

Mapping of clouston hidrotic ectodermal dysplasia

open access: yes, 1999
Clouston hidrotic ectodermal dysplasia (BED) is an autosomal dominant skin disorder that is characterized by nail dystrophy, hair defects and palmoplantar hyperkeratosis.
Kibar, Zoha D.
core  

EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia. [PDF]

open access: yes
Hypohidrotic ectodermal dysplasia is a developmental defect characterized by sparse or absent hair, missing or malformed teeth and defects in eccrine glands. Loss-of-function variants in the X-chromosomal EDA gene have been reported to cause hypohidrotic
Vidhya Jagannathan   +12 more
core   +2 more sources

Ectodermal dysplasia associated with immunodeficiency [PDF]

open access: yes
Background. Mutated genes cause immune system and ectodermal development cause a rare hereditary disorder known as ectodermal dysplasia with immunodeficiency.
Seethalekshmi, Vignesh Rishi Kumar   +1 more
core   +3 more sources

Auto-percepção dos portadores de Amelogênese Imperfeita e Displasia [PDF]

open access: yes, 2012
TCC (graduação) - Universidade Federal de Santa Catarina. Centro de Ciências da Saúde. Odontologia.A Amelogênese Imperfeita é um distúrbio hereditário caracterizado pela formação anormal de esmalte, o que gera dentes com alteração de cor, sensibilidade e
Klita, Ana Paula Haisi
core  

Ectodermal Dysplasia - Connections and Implantation

open access: yes, 2009
Ectodermal dysplasia is a disease of strong familial disposition. There is a broad scale of subtypes with more or less expressed signs. The diagnostics is of high significance as well as the associated missing teeth.
P. Prachár   +4 more
core  

Connexin30 mutations responsible for hidrotic ectodermal dysplasia cause abnormal hemichannel activity [PDF]

open access: yes, 2017
Clouston syndrome or hidrotic ectodermal dysplasia (HED) is a rare dominant genodermatosis characterized by palmoplantar hyperkeratosis, generalized alopecia and nail defects.
Barbe, Michael T.   +7 more
core  

Prosthetic rehabilitation for a patient with hypohidrotic ectodermal dysplasia: a clinical case

open access: yes
rotic ectodermal dysplasia (HED) is a hereditary syndrome, characterized by a classic triad of hypotrichosis, hypodontia and hypohidrosis. The case of an 8-year-old girl with HED presenting oligodontia and marked resorption of maxillary and mandibular ...
Guna Shekhar, Alluri RamaRaju, Chandrasekhar Rao, Sarada
core  

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