Results 111 to 120 of about 69,884 (306)
A Case of Congenital Cutis Laxa (Generalized Elastolysis)
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
OBJECTIVES Empirical fluoroquinolone therapy is widely used in treating complicated urinary tract infections (cUTIs), even in areas of high fluoroquinolone resistance.
Jennifer A. Huntington+6 more
semanticscholar +1 more source
Alternative treatments in the control of psoroptic mange in a flock of organic production sheep. [PDF]
The aim of the experiment was to verify the efficacy of the treatment of psoroptic mange in a flock of Churra sheep farmed under organic production conditions, using alternative methods. One group, C Control (N=9), was given no treatment, a second group,
de la Fuente, L.F.+2 more
core
Comprehensive clinical and molecular analysis of 12 families with type 1 recessive cutis laxa. [PDF]
Autosomal recessive cutis laxa type I (ARCL type I) is characterized by generalized cutis laxa with pulmonary emphysema and/or vascular complications. Rarely, mutations can be identified in FBLN4 or FBLN5.
Bresson, J.L.+27 more
core +1 more source
Bilateral Periareolar Nodules in an Adolescent With a History of Lymphoma
JEADV Clinical Practice, EarlyView.
Rawan Almutairi+5 more
wiley +1 more source
Looks can be deceiving : the deceptive milkcaps (Lactifluus, Russulaceae) exhibit low morphological variance but harbour high genetic diversity [PDF]
The ectomycorrhizal genus Lactifluus is known to contain many species complexes, consisting of morphologically very similar species, which can be considered cryptic or pseudocryptic.
Angelini, Claudio+9 more
core +2 more sources
Neonatal Epidermolytic Ichthyosis Caused by a KRT10 Mutation (c.467G>A, p.Arg156His): A Case Report
ABSTRACT We present a neonatal case of skin blisters and erythema. While epidermolysis bullosa was initially suspected, immunofluorescence antigen mapping and genetic testing confirmed epidermolytic ichthyosis, with a heterozygous pathogenic variant in the KRT10 gene (c.467G>A, p.Arg156His).
Elke Smits+4 more
wiley +1 more source
Unilateral Idiopathic Calcinosis Cutis: A Case Report
Calcinosis cutis is a rare disorder characterized by the deposition of calcium in the skin and subcutaneous tissue. Unilateral idiopathic calcinosis cutis has only rarely been reported in the literature.
Fahad Alsaif, Amr M. Abduljabbar
doaj +1 more source
Cutaneous tuberculosis (scrofuloderma) in a five year-old boy: Case report [PDF]
Cutaneous tuberculosis (CTB) is a rare form of extrapulmonary TB in our region. The incidence of CTB seems to be increasing in some countries. CTB continues to be one of the most elusive and difficult diagnoses to make for dermatologists practicing in ...
Dehghan, M.+2 more
core