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A rare heterozygous TRAF6 variant is associated with hypohidrotic ectodermal dysplasia


  • Funding sources
    This work was supported by a grant from WSPiA. S.A.W. was the recipient of a scholarship from the Postgraduate School of Molecular Medicine affiliated to Warsaw Medical University.

  • Conflicts of interest
    None declared.

Wieslaw Henryk Trzeciak.


Summary Background  Mutations in the genes encoding components of the tumour necrosis factor (TNF)-α-like pathway cause hypohidrotic ectodermal dysplasia (HED). It has been postulated that the TNF receptor-associated factor 6 (TRAF6) is also involved in this pathway.

Objectives  To investigate mutations in the TRAF6 gene in an individual with HED.

Methods  Genetic analysis was performed on TRAF6 in a patient with HED, her parents, her sister and 150 ethnically matched, healthy individuals.

Results  In the patient, sequencing analysis of one DNA strand revealed a deletion of eight nucleotides (c.1074–1081delCAATTTG) in the 5′ fragment of the last exon of TRAF6, while no deletion was detected in the other DNA strand indicating a heterozygous mutation. No such sequence abnormality was detected in the patient’s parents and her sister.

Conclusion  This is the first report of a heterozygous TRAF6 sequence variant associated with symptoms typical of HED.