Hypohidrotic Ectodermal Dysplasia with Immune Deficiency, Osteopetrosis and Lymphoedema - Diagnostic Tests

Diagnostic Tests

DNA-based molecular genetic diagnosis is possible. This will help distinguish between X-linked and autosomal forms of HED.

Diagnostic Tools

This section offers to professional users instruments helpful to establish the disease diagnosis. Specific entries include:

  1. model questionnaires, protocols, or checklists, which may guide clinicians and laboratory personnel in the diagnostic procedure of specific disease groups/subgroups;
  2. a list of cell biology/biochemical tools used for laboratory diagnosis of specific diseases or group of diseases;
  3. a list of molecular genetics tools, including mutational screening procedures, oligonucleotide primer sequences, PCR amplification conditions, and other details for selected diseases. In this section, you also find the link for the gene-specific page of the Weizmann Institute of Science GeneCards website (http://www.genecards.org) which is an integrated database including information on disease relationships, SNPs, gene expression, gene function and more.
  4. a mutation database with a GENESKIN updated list of the mutations identified in the genes responsible for selected diseases. A link with the gene-specific page at the Human Gene Mutation Database maintained at the University of Wales in Cardiff (www.hgmd.org) and other databases, such as the collagen database in Leicester (www.le.ac.uk/genetics/collagen), is also available.

Model Questionnaire

Ectodermal Dysplasia Questionnaire

Cell Biology Tools

To date, there isn’t any cell biology or biochemical diagnostic test for this condition.

Molecular Genetic Tools

Causative genes

IKK-gamma Genecards Logo

Mutation Database

Causative genes

IKK-gamma HGMD Logo

Here, you will find the downloadable version of the IKK-gamma mutation database. Please, note that this list contains all mutations identified in this gene also including those associated with other phenotypes.