Results 121 to 130 of about 65,412,535 (160)
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Linear Scleroderma en Coup De Sabre With Associated Neurologic Abnormalities

Pediatrics, 2006
Linear scleroderma represents a unique form of localized scleroderma that primarily affects the pediatric population, with 67% of patients diagnosed before 18 years of age. When linear scleroderma occurs on the head, it is referred to as linear scleroderma en coup de sabre, given the resemblance of the skin lesions to the stroke of a sabre.
Kristen E, Holland   +5 more
exaly   +3 more sources

Frontal Linear Scleroderma (en coup de sabre): A Case Report

Cleft Palate-Craniofacial Journal, 2022
En coup de sabre is a type of linear scleroderma which presents on the frontal or frontoparietal scalp. En coup de sabre in children is associated with asymmetric growth and progressive facial disfigurement. The purpose of this report was to present the case of a 4-year-old girl with a 2-year history of en coup de sabre.
Soo Hyang Lee, Yo Han Oh
exaly   +2 more sources

Double-Lined Frontoparietal Scleroderma en coup de sabre

open access: yesDermatology, 1999
We describe a rare case of double-lined frontoparietal scleroderma en coup de sabre. The relationship to the distribution following the lines of Blaschko is discussed.
Peter Schiller
exaly   +2 more sources

Management Options for Linear Scleroderma (“En Coup de Sabre”)

Dermatologic Surgery, 2022
BACKGROUND En coup de sabre (ECDS) is a form of linear-scleroderma, primarily affecting the face. Despite effectiveness of pharmacological interventions in the management of lesions, sequelae of cutaneous deformities are common.
Ron, Skorochod   +2 more
openaire   +2 more sources

Frontal Linear Scleroderma (en coup de sabre): A Case Report

The Cleft Palate Craniofacial Journal, 2021
En coup de sabre is an unusual variant of localized scleroderma characterized by its distinct location involving the frontoparietal region of the forehead and scalp. The authors describe a rare case of en coup de sabre in a 3-year-old boy whose disease onset was at 12 months of age.
Yo Han Oh, Soo Hyang Lee
openaire   +2 more sources

Neuroimaging is useful for monitoring disease activity in linear scleroderma "en coup de sabre".

open access: yesMinerva pediatrica, 2014
Scleroderma is a group of rare chronic connective tissue disorders characterized by collagen accumulation that causes tissue hardening with consequent fibrosis. Skin involvement is mostly frequent, although several internal organs can be impaired (heart, lungs, liver, etc.). In childhood, juvenile localized scleroderma (JLS) is more frequently observed;
CHINI, LOREDANA   +9 more
core   +4 more sources

Bilateral linear scleroderma en coup de sabre.

Archives of dermatology, 1968
Two cases of bilateral linear scleroderma en coup de sabre, one with and one without associated facial atrophy, have been presented. Bilateral involvement in this entity is rare. The relationship of bilateral linear scleroderma en coup de sabre to Romberg's progressive facial atrophy is discussed, the conclusion being that the presence of bilateral ...
J J, Dilley, H O, Perry
openaire   +3 more sources

Linear scleroderma “En Coup de Sabre” of the cheek

Journal of Oral and Maxillofacial Surgery, 2003
Linear scleroderma (LS) is a variant of localized scleroderma most commonly seen in the lower limbs and to a lesser extent in the arms and face.1 Systemic involvement in LS is extremely rare.1,2 The term “en coup de sabre” is used for linear scleroderma located in the temporoparietal region that produces sharp bordered furrowing with alopecia when ...
Demir, Y   +4 more
openaire   +2 more sources

Linear Scleroderma En Coup De Sabre Affecting the Upper Eyelid and Lashes

Graefe's Archive for Clinical and Experimental Ophthalmology, 2012
Evan H Black
exaly   +3 more sources

Hippocampal Atrophy and Developmental Regression as First Sign of Linear Scleroderma “En Coup De Sabre”

open access: yesEuropean Journal of Paediatric Neurology, 2008
An 8-year-old girl with linear scleroderma "en coup de sabre" is reported who, at preschool age, presented with intractable simple partial seizures more than 1 year before skin lesions were first noticed. MRI revealed hippocampal atrophy, controlaterally
Rik Joos, Hilde Beele
exaly   +2 more sources

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