| Literature DB >> 20151948 |
Dagmara E Y Mayer1, Christian Baal, Margaritha Litschauer-Poursadrollah, Wolfgang Hemmer, Reinhart Jarisch.
Abstract
The tricho-dento-osseous syndrome is a rare genetic disorder due to a mutation in the DLX3 gene on chromosome 17q21. It can affect hair, teeth, bone and nails, causing phenotypic variability. We report on an 8-year-old girl with tricho-dento-osseous syndrome, who presented in our allergy center with severe atopic dermatitis. Additional clinical findings included light, kinky hair reminiscent of pili trianguli et canaliculi (uncombable hair), enamel hypoplasia and enlarged pulp chambers of the molar teeth (taurodontism). A genetic investigation revealed a de-novo mutation in the DLX3 gene on chromosome 17q21. Electron microscopic examination of the curly hair showed a flattened hair shaft with longitudinal grooves.Entities:
Mesh:
Substances:
Year: 2010 PMID: 20151948 DOI: 10.1111/j.1610-0387.2009.07125_supp.x
Source DB: PubMed Journal: J Dtsch Dermatol Ges ISSN: 1610-0379 Impact factor: 5.584