Prenatal Screening for Bathing-suit Ichthyosis After Diagnosis in an Older Sibling

[1]  J. Toribio,et al.  Ictiosis congénitas autosómicas recesivas , 2013 .

[2]  C. Derbois,et al.  Specific TGM1 mutation profiles in bathing suit and self-improving collodion ichthyoses: phenotypic and genotypic data from 9 patients with dynamic phenotypes of autosomal recessive congenital ichthyosis. , 2012, Archives of dermatology.

[3]  R. González-Sarmiento,et al.  Prevalence of autosomal recessive congenital ichthyosis: a population-based study using the capture-recapture method in Spain. , 2012, Journal of the American Academy of Dermatology.

[4]  C. Bodemer,et al.  Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009. , 2010, Journal of the American Academy of Dermatology.

[5]  A. Irvine,et al.  Genotype–phenotype correlations with TGM1: clustering of mutations in the bathing suit ichthyosis and self‐healing collodion baby variants of lamellar ichthyosis , 2010, The British journal of dermatology.

[6]  H. Hennies,et al.  Transglutaminase-1 and bathing suit ichthyosis: molecular analysis of gene/environment interactions. , 2009, The Journal of investigative dermatology.

[7]  H. Hennies,et al.  Bathing suit ichthyosis is caused by transglutaminase-1 deficiency: evidence for a temperature-sensitive phenotype. , 2006, Human molecular genetics.

[8]  W. Jacyk.  Bathing-suit ichthyosis. A peculiar phenotype of lamellar ichthyosis in South African blacks. , 2005, European journal of dermatology : EJD.

[9]  P. Redondo,et al.  Topical N-acetylcysteine for lamellar ichthyosis , 1999, The Lancet.

[10]  M. Ponec,et al.  Mutations of keratinocyte transglutaminase in lamellar ichthyosis , 1995, Science.