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Cutis laxa (CL) is an inherited or acquired connective tissue disorder characterized by wrinkled, redundant and sagging inelastic skin associated with skeletal and developmental anomalies and, in some cases, with severe systemic involvement.
G W, KORTING, E, GOTTRON
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Prevalence and clinical association with calcinosis cutis in early systemic sclerosis
Modern Rheumatology, 2021Objectives Calcinosis cutis is often found with systemic sclerosis (SSc). However the calcinosis cutis and its clinical association among SSc patients is limited.
Chawiporn Muktabhant+3 more
semanticscholar +1 more source
Journal of dermatological treatment (Print), 2021
Background Xerosis cutis is recognized as a burdensome and stressful condition of the skin, resulting in impaired health-related quality of life (HRQoL).
C. C. von Stülpnagel+5 more
semanticscholar +1 more source
Background Xerosis cutis is recognized as a burdensome and stressful condition of the skin, resulting in impaired health-related quality of life (HRQoL).
C. C. von Stülpnagel+5 more
semanticscholar +1 more source
Cutis laxa: A comprehensive overview of clinical characteristics and pathophysiology
Clinical Genetics, 2020Cutis laxa (CL) syndromes comprise a rare group of multisystem disorders that share loose redundant skin folds as hallmark clinical feature. CL results from impaired elastic fiber assembly and homeostasis, and the known underlying gene defects affect ...
A. Beyens+3 more
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“Everybody loves somebody sometime.” So began the signature song of the popular American entertainer, Dean Martin. This famous lyric describes a universal fact of life, something we all experience sooner or later: falling in love. The ancient Romans believed that Cupid, the god of love, shot an arrow which inspired passion in the wounded victim.
Walter H.C. Burgdorf, Leonard J. Hoenig
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Clincal and Experimental Dermatology, 2020
Aplasia cutis congenita (ACC) is a rare, congenital disorder characterized by localized or widespread absence of skin at birth with heterogeneous clinical presentation. The classification proposed by Frieden in 1986 is widely used.
D. Sathishkumar+3 more
semanticscholar +1 more source
Aplasia cutis congenita (ACC) is a rare, congenital disorder characterized by localized or widespread absence of skin at birth with heterogeneous clinical presentation. The classification proposed by Frieden in 1986 is widely used.
D. Sathishkumar+3 more
semanticscholar +1 more source
Characterizing calcinosis cutis in a pediatric population
Pediatric dermatology, 2020Calcinosis cutis is the abnormal deposition of calcium in the skin and subcutis. There is currently a paucity of data surrounding pediatric calcinosis cutis. The objective of this study is to characterize calcinosis cutis in a pediatric cohort.
Ross Whitlock, Y. Chiu
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2013
Cutis laxa is an inherited or acquired disease characterized by redundant, sagging and inelastic skin. In inherited cutis laxa an abnormal synthesis of extracellular matrix proteins occurs due to genetic defects coding for diverse extracellular matrix components.
Mohamed, M.+6 more
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Cutis laxa is an inherited or acquired disease characterized by redundant, sagging and inelastic skin. In inherited cutis laxa an abnormal synthesis of extracellular matrix proteins occurs due to genetic defects coding for diverse extracellular matrix components.
Mohamed, M.+6 more
openaire +3 more sources