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JAMA Dermatology, 2023
This case report describes a patient in her 30s who was born with ichthyosis who presented with plate-like scale that covered her whole body as well as ectropion.
Yi-Cheng, Wu, Qiang, Yao
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This case report describes a patient in her 30s who was born with ichthyosis who presented with plate-like scale that covered her whole body as well as ectropion.
Yi-Cheng, Wu, Qiang, Yao
openaire +3 more sources
Pediatric dermatology, 2023
Therapeutic options are limited in cases of autosomal recessive congenital ichthyosis with inadequate response to topical agents. Acitretin is the current standard of care in these patients, but its use is limited by cumulative toxicity when prolonged ...
Femina Azeez +4 more
semanticscholar +1 more source
Therapeutic options are limited in cases of autosomal recessive congenital ichthyosis with inadequate response to topical agents. Acitretin is the current standard of care in these patients, but its use is limited by cumulative toxicity when prolonged ...
Femina Azeez +4 more
semanticscholar +1 more source
The New England journal of medicine, 1972
Biopsy specimens from patients with lamellar ichthyosis were studied by histologic, enzyme histochemical, and electron microscopic methods. Routine sections were not diagnostic, showing hyperkeratosis, normal or thickened granular zone, and acanthosis and papillomatosis.
+5 more sources
Biopsy specimens from patients with lamellar ichthyosis were studied by histologic, enzyme histochemical, and electron microscopic methods. Routine sections were not diagnostic, showing hyperkeratosis, normal or thickened granular zone, and acanthosis and papillomatosis.
+5 more sources
Maxillofacial rehabilitation of lamellar ichthyosis
Journal of Datta Meghe Institute of Medical Sciences University, 2022Lamellar ichthyosis (LI) is a rare genetic skin disorder that is present at birth, with an incidence of
M. Kamath +3 more
semanticscholar +1 more source
Peeling away the layers: A case of lamellar ichthyosis with severe ectropion in a newborn
Indian Journal of Ophthalmology - Case ReportsThis case report discusses a male neonate diagnosed with congenital lamellar ichthyosis (LI), characterized by hyperkeratinization and severe ectropion.
Ruchi Shukla +5 more
semanticscholar +1 more source
International Journal of Pedodontic Rehabilitation, 2021
Ichthyosis is a group of rare Mendelian disorders which affects cornification of the skin characterized by hyperkeratosis and/or scaling. The incidence of lamellar ichthyosis is estimated to be approximately 1 in 300,000 live births with no known sex ...
R. Tyagi +4 more
semanticscholar +1 more source
Ichthyosis is a group of rare Mendelian disorders which affects cornification of the skin characterized by hyperkeratosis and/or scaling. The incidence of lamellar ichthyosis is estimated to be approximately 1 in 300,000 live births with no known sex ...
R. Tyagi +4 more
semanticscholar +1 more source
Autosomal dominant lamellar ichthyosis
Clinical Genetics, 1986Five members of two generations of one family were affected with lamellar ichthyosis, suggesting autosomal dominant transmission. The clinical and histopathological characteristics of the cases described here are similar to those reported by Traupe et al.
J, Toribio +4 more
openaire +2 more sources

