Results 201 to 210 of about 72,798 (235)

Autosomal dominant lamellar ichthyosis

Clinical Genetics, 1986
Five 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.
V. Fernández Redondo, Jaime Toribio, Carmen Peteiro, J. M. Fabeiro, A. Zulaica   +4 more
openaire   +3 more sources

Maxillofacial rehabilitation of lamellar ichthyosis

Journal of Datta Meghe Institute of Medical Sciences University, 2022
Lamellar ichthyosis (LI) is a rare genetic skin disorder that is present at birth, with an incidence of
M. Kamath, Rinsha Gireesh, K. Bendale, Vignesh Kamath   +3 more
semanticscholar   +1 more source

Lamellar Ichthyosis in a Saudi Kindred

SKINmed: Dermatology for the Clinician, 2007
A series of 20 patients aged 4–16 years presented with lamellar ichthyosis at the dermatology unit of King Faisal Hospital at Taif in western Saudi Arabia. Though they had come from different families, they all belonged to the same tribe that was confined to a rural area in the precincts of Taif. The tribe is known for consanguineous marriages.
Vasanthi Ramesh, Joginder Kumar, Khalid Al Aboud, Daifullah Al Aboud   +3 more
openaire   +3 more sources

Orofacial manifestations in a child with congenital lamellar ichthyosis: Practical recommendations for dental management

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, N. Kalra, A. Khatri, P. Sabherwal, Padma Yangdol   +4 more
semanticscholar   +1 more source

Acitretin in the treatment of lamellar ichthyosis

British Journal of Dermatology, 1994
Etretinate and its metabolite acitretin have been shown to be highly effective in the treatment of various disorders of keratinization, including lamellar ichthyosis. The aim of the present study was to provide further information on acitretin dosage regimens in the management of lamellar ichthyosis.
Peter M. Steijlen, R.J. van Dooren-Greebe, P.C.M. van de Kerkhof   +2 more
openaire   +2 more sources

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

Genetics of lamellar ichthyosis

Egyptian Journal of Dermatology and Venereology
Ichthyosis is a dermatological condition that causes the skin in a wide range of integumentary regions of the body to become dry, rough, and scaly. Ichthyosis affect 5–10/100 000 people worldwide.
Ziske Maritska, Sandria Sandria, Nunung Noviyanti, U. M. Lubis, Maretha W. Astria, Merta A. Prastika, Priya A. Chandra, Raden Satria Surya Chandra   +7 more
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.
Reena Sharma, Indra Kumar Sharma, Ganesh Kumar Verma, Gunjan Jain, Vaibhav Kumar Jain   +4 more
openaire   +3 more sources

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   +3 more sources

Fibroblast apoptosis in a patient affected by lamellar ichthyosis

Journal of Cutaneous Pathology, 2009
Background:  Lamellar ichthyosis (LI) is a congenital recessive skin disorder characterized by generalized scaling and hyperkeratosis. The pathology may be caused by mutations in transglutaminase 1 (TGM1) gene that encodes an enzyme critical for terminally differentiating keratinocytes. Because of evidences that transglutaminase enzymes are involved in
Tavian Daniela, Tavian Daniela, Colombo Roberto, Colombo Roberto, Misiti Francesco, Ena Pasquale, Ena Luca, Sampaolese Beatrice, Giardina Bruno, Clementi Maria E, Clementi Maria E   +10 more
openaire   +10 more sources