Dataset Information


Hypohidrotic ectodermal dysplasia and immunodeficiency with coincident NEMO and EDA mutations.

ABSTRACT: Ectodermal dysplasias (ED) are uncommon genetic disorders resulting in abnormalities in ectodermally derived structures. Many ED-associated genes have been described, of which ectodysplasin-A (EDA) is one of the more common. The NF-?B essential modulator (NEMO encoded by the IKBKG gene) is unique in that mutations result in severe humoral and cellular immunologic defects in addition to ED. We describe three unrelated kindreds with defects in both EDA and IKBKG resulting from X-chromosome crossover. This demonstrates the importance of thorough immunologic consideration of patients with ED even when an EDA etiology is confirmed, and raises the possibility of a specific phenotype arising from coincident mutations in EDA and IKBKG.


PROVIDER: S-EPMC3341983 | BioStudies | 2011-01-01

REPOSITORIES: biostudies

Similar Datasets

2016-01-01 | S-EPMC5042395 | BioStudies
2019-01-01 | S-EPMC6700831 | BioStudies
2005-01-01 | S-EPMC3330241 | BioStudies
2017-01-01 | S-EPMC5664109 | BioStudies
2019-01-01 | S-EPMC6325906 | BioStudies
2014-01-01 | S-EPMC4190877 | BioStudies
2001-01-01 | S-EPMC34649 | BioStudies
2019-01-01 | S-EPMC6355244 | BioStudies
2004-01-01 | S-EPMC344191 | BioStudies
1000-01-01 | S-EPMC4734069 | BioStudies