De novo mutations in monilethrix

Authors


Abraham Zlotogorski, MD, Department of Dermatology, Hadassah University Medical Center, PO Box 12000, Jerusalem 91120, Israel.
Tel.: +972-2-6777111
Fax: +972-2-6432883
e-mail: zloto@cc.huji.ac.il

Abstract

Abstract: Mutations in the hair keratins hHb1 and hHb6 have been recently reported to cause monilethrix, an autosomal dominant hair shaft disorder, characterized by variable degrees of hair fragility and follicular hyperkeratosis. We found 10 families with monilethrix in which the parents were not clinically affected, and sequenced the hair keratin hHb1, hHb3 and hHb6 genes in seven patients. In five patients no mutations were found, while in two patients we identified de novo germline missense mutations at the helix termination motif: E402K (hHb6) and E413K (hHb1).

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