Results 21 to 30 of about 2,309 (169)
The diagnostic dilemma of cutis laxa: A report of two cases with genotypic dissimilarity
Indian Journal of Dermatology, 2015 Cutis laxa is a heterogeneous group of diseases, with loose, wrinkled skin folds and hyperelasticity of the skin. There are overlapping of clinical features of the group of syndrome associated with cutis laxa, including congenital cutis laxa, wrinkly ...
Manisha Goyal +3 more
doaj +1 more source
Generalized Acquired Cutis Laxa Associated with Monoclonal Gammopathy of Dermatological Significance
Case Reports in Dermatological Medicine, 2020 Background. Cutis laxa is a rare dermatosis that is inherited or acquired and clinically features loose, wrinkled, and redundant skin with decreased elasticity.
Sophia Z. Shalhout +3 more
doaj +1 more source
Caracterização das estruturas de N-glicanos de glicoproteínas plasmáticas por espectrometria de massa em distúrbios congênitos de glicosilação tipo II [PDF]
, 2016 Dissertação (mestrado) — Universidade de Brasília, Faculdade em Ciências da Saúde, Programa de Pós-Graduação em Ciências da Saúde, 2016.Os distúrbios congênitos de glicosilação tipo II (CDG II) são doenças graves, multissistêmicas, devidos a mutações ...
Fontes, Nilza do Carmo
core +1 more source
Type II acquired cutis laxa associated with recurrent urticarial vasculitis: brief report
Allergy, Asthma & Clinical Immunology, 2020 Background Cutis laxa is a connective tissue disease characterized by loose, wrinkled, and redundant skin. It is either inherited or acquired. In most cases, acquired cutis laxa is associated with neoplasms, drugs, and autoimmune diseases.
Amelia Nabatanzi +4 more
doaj +1 more source
Exercício físico na osteogênese imperfeita [PDF]
, 2014 A osteogênese imperfeita (OI) é um distúrbio hereditário do tecido conjuntivo, caracterizada por fragilidade óssea e baixa densidade óssea, com um amplo espectro de expressão clínica.
Campana, Angela Nogueira Neves Betanho +3 more
core +2 more sources
Indian Journal of Paediatric Dermatology, 2016 Marshall's syndrome is a form of acquired cutis laxa without systemic involvement. It is characterized by acute onset of multiple erythematous papule and plaques that resolve with postinflammatory elastolysis and cutis laxa.
Neha Meena +3 more
doaj +1 more source
A Case of Congenital Cutis Laxa (Generalized Elastolysis)
Canadian Respiratory Journal, 2005 Cutis laxa (generalized elastolysis) is characterized by sagging folds of loose skin on the face and trunk. Although grouped with hyperelastic skin conditions such as Ehlers-Danlos syndrome, cutis laxa shows an almost total lack of skin elasticity ...
Paul Champion, Frank Ryan
doaj +1 more source
Genetics and Molecular Biology, 2005 Two unrelated patients of different sexes are described, both presenting with congenital redundant skin (cutis laxa), growth deficiency, mental retardation and bone dystrophy.
Carlos Eduardo Steiner +2 more
doaj +1 more source
Autosomal recessive cutis laxa Type II: Report of novel mutation in a child
Indian Dermatology Online Journal, 2017 Autosomal recessive cutis laxa type-II (ARCLII) is a spectrum of clinical disorders with prenatal and postnatal growth retardation, cutis laxa, dysmorphism, and skeletal abnormalities.
Rakesh Kumar +3 more
doaj +1 more source
A 5-year journey with cutis laxa in an Indian child: The de barsy syndrome revisited
Indian Journal of Dermatology, 2016 De Barsy syndrome (DBS), synonymously known as autosomal recessive cutis laxa type III, is an extremely rare condition clinically characterized by cutis laxa, a progeroid appearance, and ophthalmologic abnormalities.
Abhijit Dutta +3 more
doaj +1 more source