Results 31 to 40 of about 737 (139)
RGUHS Journal of Medical Sciences, 2012 We report two cases of Collodion baby presented to NICU with parchment like skin which were diagnosed and managed. Initial stabilization management and nursing consideration of the neonate with impaired skin integrity leading to repeated infection is outlined with a note on antenatal ...
Muralidhar L Kulkarni +7 more
openaire +2 more sources
Cermin Dunia Kedokteran, 2022 Collodion baby (CB) is a rare dermatological condition worldwide of 1: 300.000 birth. A Collodion baby is a newborn whose entire body is covered with an adherent, supple, parchment-like membrane. Collodion baby in a manifestation of various hereditary conditions, including Harlequin orchestras’ (HI), lamelar orchestras’ (LI), non-bullous congenital ...
A. A. Made Berastia Anis Savitri, +1 more
openaire +2 more sources
Dupilumab for Trichothiodystrophy—Case Report and Review of the Literature
Clinical Case Reports, Volume 14, Issue 4, April 2026.ABSTRACT Trichothiodystrophy (TTD) arises from pathogenic changes in several genes, most of which participate in DNA repair or transcriptional and translational processes. Atopic dermatitis may accompany TTD in a minority of cases. Dupilumab can offer a safe and effective treatment option for severe atopic dermatitis in this population.
Julia O'Mahony, Cathal O'Connor
wiley +1 more source
A cross-sectional study on the prevalence and determinants of various neonatal dermatoses
Journal of Family Medicine and Primary Care, 2023 Background: During the neonatal life cycle, various dermatological conditions are common. In comparison to the skin of adults, neonates' skins are more susceptible to infections in the first week of their lives.
Sabiha Quazi +5 more
doaj +1 more source
Dupilumab Reduces Pruritus in Twins With Sjögren–Larsson Syndrome
Pediatric Dermatology, Volume 43, Issue 2, Page 395-397, March/April 2026.ABSTRACT Sjögren–Larsson Syndrome (SLS), now termed ALDH3A2‐syndromic epidermal differentiation disorder (sEDD), is a rare genetic disorder marked by thickened skin, spasticity, and intellectual disability. Intractable pruritus is a nearly universal and debilitating feature of SLS that remains poorly managed by current therapies. We describe 4‐year‐old
Kennedy Gallagher +3 more
wiley +1 more source
Congenital Bilateral Ectropion in Collodion Baby: A Rare Case Report
Delhi Journal of Ophthalmology, 2019 A baby born with normal full term vaginal delivery to a healthy mother aged 30 years was admitted to Neonatal intensive care unit at our tertiary care centre.
Aruna K.R. Gupta +4 more
doaj +1 more source
Journal of Nursing Management, Volume 2026, Issue 1, 2026.Background Continuous advancements in neonatal intensive care (NICU) have increased the complexity of care and the workload of nurses. Existing workload measurement instruments, such as the Winnipeg Assessment of Neonatal Nurses Needs Tool (WANNNT), are valuable but require adaptation to local healthcare settings.
Brenda Van Delft +12 more
wiley +1 more source
Journal of Nepal Paediatric Society, 1970 DOI = 10.3126/jnps.v28i2.1391J. Nepal Paediatr. Soc.
DR Aryal, K Subedi, SM Gurubacharya
openaire +2 more sources
Ichthyosis: case report in a Colombian man with genetic alterations in ABCA12 and HRNR genes
BMC Medical Genomics, 2021 Background Ichthyosis is a heterogeneous group of diseases caused by genetic disorders related to skin formation. They are characterized by generalized dry skin, scaling, hyperkeratosis and frequently associated with erythroderma.
Ruben D. Arias-Pérez +14 more
doaj +1 more source
Collodion Baby: A Case Report [PDF]
Journal of Perinatology, 2000 A case report of a collodion baby born in a community hospital who was diagnosed, stabilized, and transferred for dermatologic management is presented. Differential diagnosis based on cornification disorder phenotypes is outlined. The initial stabilization, management, and nursing considerations of the infant with impaired barrier function of the skin ...
M J, Shareef +4 more
openaire +2 more sources