Epidermolytic hyperkeratosis (EHK), earlier termed as bullous congenital ichthyosiform
erythroderma is a skin disorder characterized as an autosomal dominant and rare disorder …

Ichthyosis are disorders of cornification characterized clinically by a pattern of scaling and
histologically by hyperkeratosis. Babies with these conditions present as collodion babies …

Background The term “collodion baby” is used to describe a newborn covered with a
translucent, parchment-like skin sheet. It is an extremely rare condition with an estimated …

Congenital ichthyoses are relatively uncommon skin disorder s wi th worldwide occurrence.
The ichthyoses are heterogenous disorders of keratinisation characterised by scaling of the …

Harlequin ichthyosis (HI) is a rare genetic skin disorder characterized by dry, thickened,
scaly, fish-like skin with an autosomal recessive inheritance pattern. It is the severest form of …

Congenital bilateral upper eyelids eversion is rare clinical condition. However it is known to
be associated with collodion baby, Down syndrome and children of black race. This …

The moderating role of gender on genetics knowledge and perceived need for genetic
counseling on attitude to genetic counseling was examined. Three hundred and thirty-one …

Lamellar ichthyosis is a rare genetic dermatosis, mostly inherited in an autosomal recessive
fashion. Though not generally life-threatening, its distinctive features are not only distressing …

Aims: The purpose of this study is to present a case of Harlequin fetus, which is extremely
rare. Presentation of Case: A 27-year-old woman, gravida 3 para 1, was referred to the clinic …

Ichthyosis is a rare congenital disorder of the skin characterized by the presence of extra
covering of tough film-like membrane over the skin leading to fissure formation on stretching …