Results 1 to 10 of about 16,240 (205)

Early Neonatal Death in Harlequin Ichthyosis: A Case Report and Literature Review [PDF]

open access: yesClinical Case Reports
Harlequin 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.
Ahmed Alanzi   +5 more
doaj   +3 more sources

Report of a Novel ALOX12B Mutation in Self-Improving Collodion Ichthyosis with an Overview of the Genetic Background of the Collodion Baby Phenotype

open access: yesLife, 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.
Norbert Kiss   +2 more
exaly   +3 more sources

Comparison of artifacts between paste and collodion method of electrode application in pediatric EEG

open access: yesClinical 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 D Shah   +2 more
exaly   +3 more sources

Collodion phenotype remains a challenge for neonatologists: A rare case of self‐healing collodion baby

open access: yesClinical 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

Atypical case of neonatal-onset Gaucher disease type 3b: A case report [PDF]

open access: yesMolecular Genetics and Metabolism Reports
Neonatal-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)
Takanori Onuki   +7 more
doaj   +2 more sources

Lamellar Ichthyosis in a Resource-Limited Setting: A Somaliland Case Report [PDF]

open access: yesInternational Medical Case Reports Journal
Mohamed 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
doaj   +2 more sources

Targeted principle component analysis: A new motion artifact correction approach for near-infrared spectroscopy [PDF]

open access: yesJournal of Innovative Optical Health Sciences, 2014
As near-infrared spectroscopy (NIRS) broadens its application area to different age and disease groups, motion artifacts in the NIRS signal due to subject movement is becoming an important challenge. Motion artifacts generally produce signal fluctuations
Meryem A. Yücel   +3 more
doaj   +6 more sources

A novel mutation in the transglutaminase-1 gene identified in a collodion baby: A case report [PDF]

open access: yesJournal of International Medical Research
Autosomal 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 ...
Wang Lixiang   +4 more
doaj   +2 more sources

Case report of self-improving collodion ichthyosis in the newborn [PDF]

open access: yesJournal of International Medical Research, 2023
Self-improving collodion ichthyosis (SICI) is a relatively rare subtype of autosomal recessive congenital ichthyosis (ARCI) that is often characterized by a collodion baby (CB) phenotype at birth.
Suyue Zhu   +4 more
doaj   +2 more sources

Collodion baby [PDF]

open access: yesInternational Journal of Surgery Case Reports, 2023
ABSTRACT Introduction: Collodion baby “CB” is an extremely rare dermatological condition. Approximately 1 in 100,000 births are identified as infants with CB syndrome, including stillbirths (Dyer et al., 2013). A cornified substance replaces the newborn's
Bouab, Maryem   +5 more
openaire   +3 more sources

Home - About - Disclaimer - Privacy