We had the opportunity to manage a case of bilateral ectropion in a collodion baby. Collodion baby is a rare congenital disorder characterized by parchment like taught membrane covering the whole body. Incidence of this condition is 1 in 300,000 live births.1 A three months old collodion baby was referred to us for management of bilateral ectropion. An appropriate-for-gestational-age boy was born at 39 weeks ’ gestation by a normal vaginal delivery of a 27-year- female, with an unremarkable pregnancy and of a non-consangious marriage (Figure 1). On examination, the patient had bilateral ectropion of both the upper and lower eyelids. The eyelashes on the lower eyelids were missing. There was no evidence of corneal opacities or keratitis. The...
AbstractCongenital ichthyosis is a type of generalized hyperkeratinization of the skin at birth. Thr...
Colloidon baby is a rare congenital disorder characterized clinical-ly by parchment like taught memb...
Lamellar ichthyosis (LI), is a rare genodermatoses, that appears at birth and continues throughout a...
Collodion baby (CB) is a rare dermatological condition worldwide of 1: 300.000 birth. A Collodion ba...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Collodion baby is a distinct subset of neonatal erythroderma that can be a clinical marker for a var...
AIM OF THE STUDY:-To report a rare case of dermatological Anomaly that came across in an outpatient ...
Objective: This report describes a clinically rare case of congenital ectropion involving both uppe...
Ichthyosiform dermatoses are a group of hereditary disorders characterized by dryness and roughness ...
Introduction: The term collodion baby refers to a clinical entity noted in newborns who are enmeshed...
Abstract Background The term “collodion baby” is used to describe a newborn covered with a transluce...
Colloidion baby is a name given to baby born yellow, scaly wax like covering the baby. It is also kn...
Collodion baby is a rare congenital disorder resembling harlequin fetus but is milder in degree. Alt...
The purpose of this study is to report a case of bilateral congenital eversion of the upper eyelid i...
A female full term newborn was transferred, immediately after birth, to our Intensive Neonatal Care...
AbstractCongenital ichthyosis is a type of generalized hyperkeratinization of the skin at birth. Thr...
Colloidon baby is a rare congenital disorder characterized clinical-ly by parchment like taught memb...
Lamellar ichthyosis (LI), is a rare genodermatoses, that appears at birth and continues throughout a...
Collodion baby (CB) is a rare dermatological condition worldwide of 1: 300.000 birth. A Collodion ba...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Collodion baby is a distinct subset of neonatal erythroderma that can be a clinical marker for a var...
AIM OF THE STUDY:-To report a rare case of dermatological Anomaly that came across in an outpatient ...
Objective: This report describes a clinically rare case of congenital ectropion involving both uppe...
Ichthyosiform dermatoses are a group of hereditary disorders characterized by dryness and roughness ...
Introduction: The term collodion baby refers to a clinical entity noted in newborns who are enmeshed...
Abstract Background The term “collodion baby” is used to describe a newborn covered with a transluce...
Colloidion baby is a name given to baby born yellow, scaly wax like covering the baby. It is also kn...
Collodion baby is a rare congenital disorder resembling harlequin fetus but is milder in degree. Alt...
The purpose of this study is to report a case of bilateral congenital eversion of the upper eyelid i...
A female full term newborn was transferred, immediately after birth, to our Intensive Neonatal Care...
AbstractCongenital ichthyosis is a type of generalized hyperkeratinization of the skin at birth. Thr...
Colloidon baby is a rare congenital disorder characterized clinical-ly by parchment like taught memb...
Lamellar ichthyosis (LI), is a rare genodermatoses, that appears at birth and continues throughout a...