Overview

ectodermal dysplasia


Related Overviews

 

'ectodermal dysplasia' can also refer to...

ectodermal dysplasia

ectodermal dysplasia

anhidrotic ectodermal dysplasia

hypohidrotic ectodermal dysplasia n.

ectodermal dysplasia n.

XLID-Choroideremia-Ectodermal Dysplasia (van den Bosch Syndrome)

X-Linked Ectodermal Dysplasia in the Dog

ectodermal dysplasia with ectrodactyly and macular dystrophy

Osteopetrosis, Ectodermal Dysplasia, Immune Defect (Mim 300301)

ectodermal dysplasia with ectrodactyly and macular dystrophy

The Ectodysplasin Signaling Pathway in Hypohidrotic Ectodermal Dysplasias

Genetic Mapping of Canine Multiple System Degeneration and Ectodermal Dysplasia Loci

Connexin30 mutations responsible for hidrotic ectodermal dysplasia cause abnormal hemichannel activity

Anhidrotic Ectodermal Dysplasia (EDA) Protein Expressed in MCF-7 Cells Associates with Cell Membrane and Induces Rounding

The Anhidrotic Ectodermal Dysplasia Gene (EDA) Undergoes Alternative Splicing and Encodes Ectodysplasin-A with Deletion Mutations in Collagenous Repeats

The Gene Responsible for Clouston Hidrotic Ectodermal Dysplasia Maps to the Pericentromeric Region of Chromosome 13q

The NF-κB signalling pathway in human diseases: from incontinentia pigmenti to ectodermal dysplasias and immune-deficiency syndromes

Ectrodactyly -Ectodermal Dysplasia-Cleft Lip/Palate Syndrome and Isolated Ectrodactyly (Mim 129900; 604292; 119100; 313350; 600095; 605289; 603273; 225300)

TP63 and the Ectodermal Dysplasia, Ectrodactyly, and Cleft Lip and/or Palate (EEC), Limb-Mammary (LMS), Ankyloblepharon, Ectrodactyly, and Cleft Lip/Palate (AEC, Hay-Wells), Acro-Dermato-Ungual-Lacrimal-Digit (ADULT), and Rapp-Hodgkin Syndromes and Ectrodactyly (Split Hand/Foot Malformation)

 

More Like This

Show all results sharing this subject:

  • Medicine and Health

GO

Show Summary Details

Quick Reference

Hypohidrotic ectodermal dysplasia, a congenital disorder of teeth, hair, and eccrine sweat glands, is usually inherited as an X-linked recessive trait, although rarer autosomal dominant and autosomal recessive forms are known. See IκB. McGrath's syndrome (ectodermal dysplasia syndrome) is caused by mutations in the plakophilin-1 gene. See desmosome; ectodysplasin.

Subjects: Medicine and Health.


Reference entries

Users without a subscription are not able to see the full content. Please, subscribe or login to access all content.