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Differential patterns of filaggrin expression in lamellar ichthyosis
British Journal of Dermatology, 1998Lamellar ichthyosis (LI) is a rare genetic and congenital disturbance of keratinization that is phenotypically and genotypically heterogeneous. Filaggrin is one of the major components of the stratum corneum situated in the protein matrix and the cornified envelope.
Valle +6 more
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Cutis laxa and lamellar ichthyosis in siblings
Clinical Genetics, 1976Cutis laxa and lamellar ichthyosis are two rare, genetically‐determined skin disorders. The pedigree reported represents the first documentation of the occurrence of these two disorders in a single sibship.
Nancy B. Esterly +2 more
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Lamellar Ichthyosis and Congenital Ectropion
Archives of Ophthalmology, 1990James H. Oestreicher +1 more
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Surgical Correction of Ectropion in Lamellar Ichthyosis
Annals of Plastic Surgery, 1982Menachem R. Wexler +2 more
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Anesthetic challenges in lamellar ichthyosis
Pediatric Anesthesia, 2012Varadraj V. Pai +2 more
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Bilateral pseudoainhum in lamellar ichthyosis
Pediatric Dermatology, 2004V. Ramesh +2 more
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Molecular understanding of lamellar ichthyosis
Journal of the European Academy of Dermatology and Venereology, 1995openaire +2 more sources