A CASE REPORT: LAMELLAR ICHTHYOSIS
نویسندگان
چکیده
منابع مشابه
A Case Report of Harlequin Ichthyosis
Harlequin ichthyosis is the most severe form of congenital ichthyoses with horny (Keratinized) and chapped thick skin throughout the body. In this disease, disruption in keratinization of epidermis results in the impaired barrier function and susceptibility of the neonate to dehydration and infection. In this article, a term male neonate with harlequin ichthyosis, born of a 29-year-old mother, ...
متن کاملHarlequin ichthyosis: A case report from Iran
Harlequin ichthyosis is a rare and exceedingly severe form of congenital ichthyosis with an incidence of approximately 1 in 300,000 births. These patients are at a high risk for neonatalinfection and septicemia. Most affected infants die within the first days or weeks of life.We report a male baby born with harlequin ichthyosis. There is limited information regarding the course and...
متن کاملLamellar 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 ...
متن کاملHarlequin ichthyosis: Case report
Harlequin fetus is a rare and the most severe form of the congenital ichthyosis with an autosomal recessive inheritance. Incidence of the disease is nearly 1 in 3,00,000 live births. The disease might be lethal at birth and the affected babies are often premature. Harlequin ichthyosis (HI) is marked by severe keratinized and alligator-like horned skin. The present study reports a new case with ...
متن کاملReport of a Congenital Ichthyosis
A case of congenital ichthiosis 1s presented. Histologic pattern and the treatment is discussed.
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ژورنال
عنوان ژورنال: International Journal of Advances in Pharmacy and Biotechnology
سال: 2017
ISSN: 2454-8375
DOI: 10.38111/ijapb.20170302002