Results 211 to 220 of about 72,798 (235)

Ponatinib‐induced lamellar ichthyosis‐like eruption

International Journal of Dermatology, 2020
Dear Editor, Tyrosine kinase inhibitors (TKI) have significantly improved the outcome and survival in patients of leukemia. However, these agents are frequently associated with mucocutaneous adverse effects including, but not limited to, cutaneous rash ...
V. Thakur, P. Malhotra, D. Lad, D. Chatterjee, K. Vinay, S. Dogra   +5 more
semanticscholar   +1 more source

Lamellar ichthyosis with laminated membrane structures

British Journal of Dermatology, 1993
Summary We review the published classifications of autosomal recessive congenital ichthyosis. and report a newcase of congenital ichthyosis which presents the characteristics of ichthyosis congenita type III.In 1988 Arnold cm/.' de.scribed a new type of congenitalichthyosis (ichthyosis congenita.
Iria Neri, V. Di Lernia, Gianandrea Pasquinelli, Annalisa Patrizi, L. Badiali De Giorgi   +4 more
openaire   +3 more sources

Molecular profiling of lamellar ichthyosis pathogenic missense mutations on the structural and stability aspects of TGM1 protein

Journal of Biomolecular Structure and Dynamics, 2020
Lamellar ichthyosis (LI) is a rare inherited disease where affected infants present a extensive skin scaling characterized by hyperkeratosis. Inherited mutations in the Transglutaminase 1 (TGM1) protein is one of the known causative genetic factor for ...
K. Nasser, B. Banaganapalli, Thoraia Shinawi, R. Elango, N. A. Shaik   +4 more
semanticscholar   +1 more source

Microbial keratitis in a case of lamellar ichthyosis

International Ophthalmology, 2007
We report a case of microbial keratitis in a patient with lamellar ichthyosis. An 11-year-old boy, a known case of lamellar ichthyosis, presented with microbial keratitis. Microbiological evaluation of corneal scraping revealed a mixed infection caused by gram-negative bacilli and gram-positive cocci.
Sujata Das, Balasubramanya Ramamurthy, Sunita Chaurasia   +2 more
openaire   +3 more sources

Lamellar Exfoliation of the Newborn, or Ichthyosis Congenita

Archives of Pediatrics & Adolescent Medicine, 1959
A baby who was born with a collodion-like membrane over the entire body has recently been under our observation. We used the term "lamellar exfoliation of the newborn" introduced by Grass and Torok 1 but observed the baby for two years before establishing a final diagnosis.
Nadine G. Smith, Northrop Beach
openaire   +3 more sources

Cicatricial Ectropion Associated With Lamellar Ichthyosis

Archives of Ophthalmology, 1973
An 8-year-old boy with lamellar ichthyosis had bilateral cicatricial ectropion of the lower eyelids. His entire body was affected including the palms and soles. Post auricular grafts were successfully used to repair the ectropion. Of the four categories of ichthyosis, the lamellar type is associated with the presence of ectropion and the resultant ...
Richard D. Shindle, Charles R. Leone
openaire   +3 more sources

Ocular Manifestations of Congenital Lamellar Ichthyosis

European Journal of Ophthalmology, 2005
Purpose To describe the ophthalmic manifestations in a series of children with congenital lamellar ichthyosis. These cases presented with varying types of eyelid abnormality associated with the systemic disease. The clinical features and ophthalmic management were studied.
A J Singh, P L Atkinson
openaire   +3 more sources

Mutations of Keratinocyte Transglutaminase in Lamellar Ichthyosis

Science, 1995
Lamellar ichthyosis is a severe congenital skin disorder characterized by generalized large scales and variable redness. Affected individuals in three families exhibited drastically reduced keratinocyte transglutaminase (TGK) activity.
Sjan Lavrijsen, Daniel Hohl, Anita Bon, Marcel Huber, Katja Bernasconi, Daniel F. Schorderet, Maria Ponec, Irmingard Rettler, Edgar Frenk, Stefan Lautenschlager   +9 more
openaire   +3 more sources

Differential patterns of filaggrin expression in lamellar ichthyosis

British Journal of Dermatology, 1998
Lamellar 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, GarcÍA Salgado, Becker, Unamuno PÉrez, Peña Penabad, PÉrez Arellano, Gutierrez De Diego   +6 more
openaire   +4 more sources

Cutis laxa and lamellar ichthyosis in siblings

Clinical Genetics, 1976
Cutis 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, Qlia I. Kaye, Carol W. Bocth   +2 more
openaire   +3 more sources