Expedient Treatment of a Collodion Baby [PDF]
Case Reports in Dermatological Medicine, 2011 Only ~270 cases of collodion babies have been reported in the literature since 1892. As the name suggests, the term “collodion baby” refers to a phenotype that can be characterized by a yellow, shiny, tight parchment-like membrane stretched over the skin.
Andrew S Chung, Nirmala Desai
exaly +8 more sources
Collodion phenotype remains a challenge for neonatologists: A rare case of self‐healing collodion baby [PDF]
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 +4 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 [PDF]
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.
Norbert Kiss +2 more
exaly +5 more sources
Acral self-healing collodion baby: A case series [PDF]
International Journal of Women's Dermatology, 2016 Collodion baby is a term used to describe a phenotype characterized by the presence of a tight, translucent membrane that covers the entire skin at birth.
Bruno Ferrari +2 more
exaly +5 more sources
Myelodysplastic Syndrome Presenting as Amegakaryocytic Thrombocytopenia in a Collodion Baby [PDF]
Journal of Investigative Medicine High Impact Case Reports, 2015 We report a rare case of myelodysplastic syndrome that presented early as amegakaryocytic thrombocytopenia in a collodion baby, which is a rare congenital disorder characterized by thick, taut membrane resembling oiled parchment or collodion, which is ...
Ehab Hanafy
exaly +4 more sources
A novel mutation in the transglutaminase-1 gene identified in a collodion baby: A case report [PDF]
Journal of International Medical ResearchAutosomal 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, Xianghong Li
exaly +4 more sources
Holocarboxylase Synthetase Deficiency: Clinical, Biochemical and Molecular Findings in Five Malaysian Patients Including a Newborn Presenting as Collodion Baby [PDF]
JIMD ReportsHolocarboxylase synthetase (HLCS) is a rare autosomal recessive disorder of biotin metabolism. The mutation spectrum is known to correlate with clinical phenotypes and responsiveness to biotin therapy. Five patients diagnosed with HLCS deficiency between
Siew Li Ting +4 more
doaj +3 more sources
Early Neonatal Death in Harlequin Ichthyosis: A Case Report and Literature Review [PDF]
Clinical Case ReportsHarlequin 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
Collodion baby with polydactyly [PDF]
Indian Dermatology Online Journal, 2015 Iffat Hassan +2 more
doaj +4 more sources