Volume 24, Issue 4 (1-2019)                   Back to this Issue | Back to browse issues page

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faal G, rabani F, Hosseini M. A case report of harlequin ichthyosis with a favorable outcome: Early treatment and significant recovery . Hayat. 2019; 24 (4) :335-341
URL: http://hayat.tums.ac.ir/article-1-2377-en.html
1- Dept. of Pediatric, School of Medicine, Birjand University of Medical Sciences, Birjand, Iran
2- Dept. of Medical Surgical Nursing, School of Nursing and Midwifery, Birjand University of Medical Sciences, Birjand, Iran , rabani_nurse@yahoo.com
3- Dept. of Medical Surgical Nursing, School of Nursing and Midwifery, Birjand University of Medical Sciences, Birjand, Iran
Abstract:   (740 Views)
Harlequin ichthyosis is the most severe form of autosomal-recessive congenital ichthyoses with a high mortality rate. In affected infants, mutations occur in the ABCA12 gene. The ABCA12 gene produces the proteins that are essential for the natural development of skin cells. In this disease, disruption in keratinization of epidermis results in the impaired barrier function and susceptibility of the neonate to dehydration and infection. Recent advances in neonatal care and early administration of treatment have increased the chances of child survival. In this article, we introduced a term female neonate with harlequin ichthyosis, born of a 26-year-old mother, significantly recovered by early treatment using an ointment (composed of Eucerin 88 g, sodium chloride 6 g, and urea 6 g).
 
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Type of Study: Case Report | Subject: Nursing Care
Published: 2019/02/27 | ePublished: 2019/02/27

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