Ichthyosis Congenita

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Ichthyosis congenita, harlequin fetus type: a case report.

Ichthyosis is a very heterogeneous family of skin disorders with harlequin ichthyosis being the most severe genetic form. It is a rare autosomal recessive condition, characterized by dry, severely thickened skin with large plates of hyperkeratotic scale, separated by deep fissures. Infants are very susceptible to metabolic abnormalities and infections. They usually do not survive for very long,...

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Aplasia cutis congenita

The patient was a female neonate bornprematurely at 36 weeks of gestation by a Cesareansection. During pregnancy, the mother had nohistory of fever, drug use, or X-ray exposure.The mother was gravida 2 and had no history ofabortion. Her first child was healthy. There wasno record of birth trauma. The perinatal historywas negative for intrauterine trauma, the use ofantithyroid medication, or mis...

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Report of a Congenital Ichthyosis

A case of congenital ichthiosis 1s presented. Histo­logic pattern and the treatment is discussed. 

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Autosomal recessive congenital ichthyosis.

The term autosomal recessive congenital ichthyosis (ARCI) refers to a group of rare disorders of keratinization classified as nonsyndromic forms of ichthyosis. This group was traditionally divided into lamellar ichthyosis (LI) and congenital ichthyosiform erythroderma (CIE) but today it also includes harlequin ichthyosis, self-healing collodion baby, acral self-healing collodion baby, and bathi...

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Heredity in Ichthyosis

A case of advanced ichthyosis was recently admitted into the Windham Hospital. The family history as far as it could be elicited made it apparent that it was a disease of the males in the family transmitted through the females, the latter being immune. The patient's elder brother was suffering from the same disease, while his sisters were all free; his father did not suffer from it, nor his gra...

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ژورنال

عنوان ژورنال: Proceedings of the Royal Society of Medicine

سال: 1950

ISSN: 0035-9157

DOI: 10.1177/003591575004300206