Lamellar ichthyosis with severe bilateral ectropion and self-healing collodion membrane

A New Born with Lamellar ichthyosis(Collodion Baby).

Ichthyosisis an infrequent clinical entity worldwide with an incidence of 1:600,000 births. It can be one of the two types: collodion baby and Harlequin fetus or malignant keratoma (most severe form). The clinical manifestations in either form are thick and hard skin with deep splits. Affected babies are born in a collodion membrane, a shiny waxy outer layer to the skin that is shed 10 - 14 day...

Collodion skin in the neonate due to lamellar ichthyosis.

Lamellar Ichthyosis with Rickets

Lamellar ichthyosis (LI) is a rare genetic disorder with autosomal recessive inheritance. It is equally seen in both sexes and usually manifests at birth. The child presents as a collodion baby. The erythema is minimal or absent; but when present, it is maximum on the face. The scaling is generalized, accentuated on lower extremities and flexural areas. Rickets is a condition in which there is ...

Scanning electron microscopy of the collodion membrane from a self-healing collodion baby*

Self-healing collodion baby is a well-established subtype of this condition. We examined a male newborn, who was covered by a collodion membrane. The shed membrane was examined with scanning electron microscopy. The outer surface showed a very compact keratin without the normal elimination of corneocytes. The lateral view of the specimen revealed a very thick, horny layer. The inner surface sho...

Lamellar ichthyosis presenting as bilateral spontaneous corneal perforation.

INTRODUCTION Lamellar Ichthyosis is an autosomal recessive, inherited skin disorder characterized by thickening, fissuring and scaling of the skin. OBJECTIVE To report a case of lamellar icthyosis and highlight the importance of monitoring corneal health in these patients. CASE We report a rare case of bilateral spontaneous corneal perforation in a patient with lamellar ichthyosis .The pati...