An unusual distribution of lamellar ichthyosis in 13 Black patients from 9 families is described. The trunk and upper extremities were mainly affected. In all patients, the temples were affected to a greater or lesser degree. The skin of the face, lower extremities, hands and feet was normal. In 1 patient the entire forehead was affected, and the skin of the upper and lower extremities showed patchy ichthyotic changes. Histologically and electron-microscopically, the picture is similar to that of lamellar ichthyosis (non-bullous congenital ichthyosiform erythroderma). Chromosamal studies in a few cases showed no abno
Non-bullous congenital ichthyosi-form erythroderma is an autosomal recessive congenital keratinizati...
Lamellar ichthyosis (LI) is a Greek phrase that literally means ‘the skin of a fish’. It is a rare a...
Here, we report a case of a middle-aged woman presenting with severe, long-standing, hyperkeratotic ...
Introduction: Ichthyosis is a heterogeneous group of skin disease characterized by generalized scali...
Ichthyosiform dermatoses are a group of hereditary disorders characterized by dryness and roughness ...
Ichthyosis is a genetically and phenotypically heterogeneous disease that can be isolated and restr...
Abstrak Iktiosis lamelaris adalah kelainan autosomal resesif yang jarang terjadi. Ditandai oleh memb...
ABSTRACT The lamellar ichthyosis is a genodermatosis autosomal recessive, rare, of variable expressi...
The first two cases of dyskeratosis congenita recognised in South Africa are described. An iron defi...
AbstractIchthyosis is a genetically and phenotypically heterogeneous disease that can be isolated an...
Hereditary ichthyosis is a collective name for many dry and scaly skin disorders ranging in frequenc...
<em style="color: #29363d; font-family: Tahoma, Arial, Helvetica, sans-serif; font-size: 14.66666698...
Vohwinkel syndrome belongs to the group of hereditary palmoplantar keratoderma, having an autosomal ...
Two cases of Sjogren-Larsson syndrome are discussed along with a review of the literature. Both the ...
A 50-year-old man presented with congenital scaling and hyperkeratosis on his palms, the soles of hi...
Non-bullous congenital ichthyosi-form erythroderma is an autosomal recessive congenital keratinizati...
Lamellar ichthyosis (LI) is a Greek phrase that literally means ‘the skin of a fish’. It is a rare a...
Here, we report a case of a middle-aged woman presenting with severe, long-standing, hyperkeratotic ...
Introduction: Ichthyosis is a heterogeneous group of skin disease characterized by generalized scali...
Ichthyosiform dermatoses are a group of hereditary disorders characterized by dryness and roughness ...
Ichthyosis is a genetically and phenotypically heterogeneous disease that can be isolated and restr...
Abstrak Iktiosis lamelaris adalah kelainan autosomal resesif yang jarang terjadi. Ditandai oleh memb...
ABSTRACT The lamellar ichthyosis is a genodermatosis autosomal recessive, rare, of variable expressi...
The first two cases of dyskeratosis congenita recognised in South Africa are described. An iron defi...
AbstractIchthyosis is a genetically and phenotypically heterogeneous disease that can be isolated an...
Hereditary ichthyosis is a collective name for many dry and scaly skin disorders ranging in frequenc...
<em style="color: #29363d; font-family: Tahoma, Arial, Helvetica, sans-serif; font-size: 14.66666698...
Vohwinkel syndrome belongs to the group of hereditary palmoplantar keratoderma, having an autosomal ...
Two cases of Sjogren-Larsson syndrome are discussed along with a review of the literature. Both the ...
A 50-year-old man presented with congenital scaling and hyperkeratosis on his palms, the soles of hi...
Non-bullous congenital ichthyosi-form erythroderma is an autosomal recessive congenital keratinizati...
Lamellar ichthyosis (LI) is a Greek phrase that literally means ‘the skin of a fish’. It is a rare a...
Here, we report a case of a middle-aged woman presenting with severe, long-standing, hyperkeratotic ...