Literature DB >> 21738992

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Isabella Brasil Succi1, Fernando Colonna Rosman, Elisa Fontenelle de Oliveira.   

Abstract

Bloch-Sulzberger syndrome (incontinentia pigmenti) is a rare genodermatosis that affects predominantly females, since it is generally lethal to male fetuses in utero. It is characterized principally by skin lesions, but may also involve dental, ophthalmological and neurological abnormalities. The skin lesions are present in four different phases: vesicular, verrucous, hyperpigmented and atrophic/hypopigmented. Their sequence is irregular and overlapping of stages is common.

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Year:  2011        PMID: 21738992     DOI: 10.1590/s0365-05962011000300037

Source DB:  PubMed          Journal:  An Bras Dermatol        ISSN: 0365-0596            Impact factor:   1.896


  1 in total

1.  Cephalometric skeletal evaluation of patients with Incontinentia Pigmenti.

Authors:  Marcia Angelica Peter Maahs; Ana Elisa Kiszewski; Rafael Fabiano Machado Rosa; Fernanda Diffini Santa Maria; Frederico Ballvé Prates; Paulo Ricardo Gazzola Zen
Journal:  J Oral Biol Craniofac Res       Date:  2014-08-22
  1 in total

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