Results 1 to 10 of about 12,465 (227)
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 +3 more sources
A novel mutation in the transglutaminase-1 gene identified in a collodion baby: A case report [PDF]
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 +3 more sources
Case report of self-improving collodion ichthyosis in the newborn [PDF]
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 +3 more sources
Early Neonatal Death in Harlequin Ichthyosis: A Case Report and Literature Review [PDF]
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
Atypical case of neonatal-onset Gaucher disease type 3b: A case report [PDF]
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
This 7 years old male child is a case of collodion baby who goes to school. He is having high hypermetropia with esotropia and bilateral lower lid ectropions.
Iftikhar Ahmad
doaj +2 more sources
An infant with lamellar ichthyosis presenting with meningitis [PDF]
Lamellar ichthyosis is a rare congenital disorder characterized by widespread epidermal hyperkeratinization. It is a rare clinical disorder throughout the entire planet, and newborns with this disease frequently have collodion membranes (adhering, supple,
Telila Mesfin +10 more
doaj +2 more sources
Collodion baby: A rare case report. [PDF]
Bouab M +5 more
europepmc +2 more sources
Acute management of constriction bands in a newborn with collodion membrane with early manual release [PDF]
Ania Stolarczyk, BS +3 more
doaj +2 more sources

