Results 201 to 210 of about 6,529 (236)

A rare case of ocular pterygium in a young boy with congenital lamellar ichthyosis

Indian Journal of Ophthalmology - Case Reports
Congenital lamellar ichthyosis is a rare dermato-ocular disease occurring in 1:300,000 population and is autosomal recessive. The most common ocular manifestation reported is cicatricial ectropion.
Shubratha S Hegde, Sandhya Dharwadkar, K. Athira, Harsha Shaji   +3 more
semanticscholar   +1 more source

Cyclosporine in lamellar ichthyosis.

Archives of dermatology, 1989
In an open trial, five patients with lamellar ichthyosis showed no response to four weeks of treatment with oral cyclosporine (cyclosporine A) (6 mg/kg/d). Histologic examination of lamellar ichthyosis revealed hyperkeratosis; psoriasiform acanthosis; dilated, tortuous capillaries; and a slight perivascular lymphocytic infiltrate.
V C, Ho, A K, Gupta, C N, Ellis, K D, Cooper, B J, Nickoloff, J J, Voorhees   +5 more
openaire   +3 more sources

Tralokinumab and Acitretin for the Treatment of Lamellar Ichthyosis.

JAMA dermatology
This case report describes a man in his 30s who presented with severe and generalized congenital ichthyosis and was treated with a combination of tralokinumab and acitretin.
A. De Greef, Marie Baeck
semanticscholar   +1 more source

Lamellar ichthyosis with bilateral ectropion

Nigerian Journal of Ophthalmology, 2015
Lamellar ichthyosis is a rare congenital disorder with ocular manifestation resulting from the cicatrization of anterior lamella of eyelids. Early diagnosis and management of ectropion can prevent the most severe complications such as severe dry eyes, corneal perforation, and possible loss of the eye.
Jain, Gunjan, Jain, Vaibhav Kumar, Sharma, Reena, Sharma, Indra Kumar, Verma, Ganesh Kumar   +4 more
openaire   +2 more sources

Lamellar Ichthyosis

Pediatrics In Review, 1981
Congenital ichthyoses represent a heterogeneous group of rare skin diseases. The disorders are heritable and have in common a varying degree of hyperkeratosis. During the years there has been much confusion regarding the classification of the ichthyoses.
openaire   +1 more source

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

Lamellar Ichthyosis and Psoriasis

Archives of Dermatology, 1973
To the Editor.— The following is an unusual presentation of two epidermal disorders in one patient. Report of a Case A 21-year-old man with a past history of lamellar ichthyosis was first seen in the University Hospital at San Diego with a three week history of a papulosquamous eruption on the trunk, extremities (including the elbows), and scalp. At
openaire   +2 more sources

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

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 ...
R D, Shindle, C R, Leone
openaire   +2 more sources

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.
A, Patrizi, I, Neri, V, Di Lernia, G, Pasquinelli, L, Badiali de Giorgi   +4 more
openaire   +2 more sources