Literature DB >> 6500829

Ozena as presenting symptom of a rare and severe genetic disease: hypohidrotic ectodermal dysplasia.

A Martini, G Magnan, A Peserico.   

Abstract

Ozena is quite a common clinical finding in ENT practice in many countries, but even if the pathological picture is clear, its etiology is unknown. We report on two young females in which ozena was the presenting symptom of a rare and severe genetic disorder (hypohidrotic ectodermal dysplasia, HED). Etiopathogenetic theories on ozena and genetic problems of HED are discussed.

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Year:  1984        PMID: 6500829     DOI: 10.1016/s0165-5876(84)80030-0

Source DB:  PubMed          Journal:  Int J Pediatr Otorhinolaryngol        ISSN: 0165-5876            Impact factor:   1.675


  3 in total

Review 1.  Ectodermal dysplasia.

Authors:  J F Masse; R Pérusse
Journal:  Arch Dis Child       Date:  1994-07       Impact factor: 3.791

2.  Role of ectodysplasin signalling in middle ear and nasal pathology in rat and mouse models of hypohidrotic ectodermal dysplasia.

Authors:  Jorge Del-Pozo; Neil MacIntyre; Ali Azar; Denis Headon; Pascal Schneider; Michael Cheeseman
Journal:  Dis Model Mech       Date:  2019-04-25       Impact factor: 5.758

3.  Ectodysplasin signalling deficiency in mouse models of hypohidrotic ectodermal dysplasia leads to middle ear and nasal pathology.

Authors:  Ali Azar; Chiara Piccinelli; Helen Brown; Denis Headon; Michael Cheeseman
Journal:  Hum Mol Genet       Date:  2016-07-04       Impact factor: 6.150

  3 in total

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