Literature DB >> 17504703

[Trichothiodystrophy: PIBIDS syndrome].

R Jiménez-Puya1, J C Moreno-Giménez, F Camacho-Martínez, J Ferrando-Barbera, R Grimalt.   

Abstract

Trichothiodystrophy comprises a heterogeneous group of autosomal recessive entities. This fact gives rise to different interrelated neuroectodermal disorders. From a structural point of view these features are the result of the low tissue sulfur content. We report a case of trichothiodystrophy initially classified as Tay syndrome that based on clinical features, complementary exams as well as on the disease evolution was labelled as PIBIDS syndrome.

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Year:  2007        PMID: 17504703

Source DB:  PubMed          Journal:  Actas Dermosifiliogr        ISSN: 0001-7310


  2 in total

1.  Do you know this syndrome? Ichthyosis associated with neurological condition and alteration of hairs.

Authors:  Luciana Baptista Pereira; Neusa Yuriko Sakai Valente; Vanessa Barreto Rocha
Journal:  An Bras Dermatol       Date:  2018 Jan-Feb       Impact factor: 1.896

2.  Trichothiodystrophy: role of a dermato-trchologist.

Authors:  Fatemeh Livani; Naser Tayebi Meibodi; Omid Rajabi; Farah Ashrafzadeh; Pouran Layegh
Journal:  Int J Trichology       Date:  2013-04
  2 in total

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