Results 1 to 10 of about 9,094 (112)
Life, 2021 Collodion baby is a congenital, transient phenotype encountered in approximately 70–90% of autosomal recessive congenital ichthyosis and is an important entity of neonatal erythroderma.
Nikoletta Nagy +2 more
exaly +3 more sources
Comparison of artifacts between paste and collodion method of electrode application in pediatric EEG
Clinical Neurophysiology Practice, 2020 Objectives: Children pose challenges to obtain quality EEG data due to excessive artifact. Collodion is used in EEG electrodes due to its water resistance and strong adhesive qualities. This study was done to evaluate differences in artifacts between the
Yash Shah +2 more
exaly +3 more sources
Clinical Case Reports (discontinued), 2022 We report a unique case of self‐healing collodion baby (CB) that was successfully managed despite the risk of potentially serious complications. Self‐healing CB is a rare and distinct outcome of collodion phenotype occurring in approximately 10% of the ...
Nikolina Zdraveska
exaly +2 more sources
Lamellar Ichthyosis in a Resource-Limited Setting: A Somaliland Case Report. [PDF]
Int Med Case Rep JMohamed Osman Aw Hashi,1,2 Ahmed M Derie,3 Sadam Ismail Ahmed4 1College of medicine and surgery, University of Hargeisa, Hargeisa, Somaliland; 2Department of Dermatology and Venereology, Hargeisa Group Hospital, Hargeisa, Somaliland; 3Department of ...
Aw Hashi MO, Derie AM, Ahmed SI.
europepmc +2 more sources
Atypical case of neonatal-onset Gaucher disease type 3b: A case report. [PDF]
Mol Genet Metab RepNeonatal-onset Gaucher disease (nGD) is considered perinatal lethal GD, a variant of GD type 2 (GD2), and is associated with collodion skin or hydrops fetalis, hepatosplenomegaly, and involvement of central nervous system (CNS). Pulmonary involvement (PI)
Onuki T +7 more
europepmc +2 more sources
A novel mutation in the transglutaminase-1 gene identified in a collodion baby: A case report. [PDF]
J Int Med ResAutosomal recessive congenital ichthyosis is a group of skin disorders characterized by abnormal keratinization. The collodion baby phenotype is a rare phenotype of autosomal recessive congenital ichthyosis characterized by a tight, translucent membrane ...
Lixiang W +4 more
europepmc +2 more sources
Early Neonatal Death in Harlequin Ichthyosis: A Case Report and Literature Review. [PDF]
Clin Case RepHarlequin ichthyosis is a rare, life‐threatening neonatal disorder often mistaken for collodion baby. We report a 37‐week neonate with severe ectropion, eclabium, and thick fissured scales who died on Day 2 despite optimal care.
Alanzi A +5 more
europepmc +2 more sources
Journal of Pathology Informatics, 2021 Background: Digital pathology has been increasingly implemented for primary surgical pathology diagnosis. In our institution, digital pathology was recently deployed in the gynecologic (GYN) pathology practice.
Iny Jhun +11 more
doaj +1 more source
A Rare Case Report of a Collodion Baby with Severe Hypernatremia [PDF]
Iranian Journal of Neonatology, 2017 Background: Collodion baby is a rare condition (i.e., 1:300000 birth), which is referred to a neonate covered with a tight and shiny membrane desquamating within two weeks.
Ahmad Farhat +3 more
doaj +1 more source
Collodion Baby: A Clinical Enigma [PDF]
Indian Journal of Neonatal Medicine and Research, 2019 Collodion baby is a term used for neonates in whom the body surface is covered by thick skin sheets, appearing like a translucent, tight parchment paper.
Sonam Singh +4 more
doaj +1 more source